Our Top Choice Compound:Benzoic anhydride

Application In Synthesis of Benzoic anhydride. About Benzoic anhydride, If you have any questions, you can contact Cao, XS; Chen, ZX; Gong, SL; Pan, K; Zhou, CJ; Huang, T; Chai, DY; Zhan, Q; Li, NQ; Zou, Y; Liu, H; Yang, CL or concate me.

Application In Synthesis of Benzoic anhydride. I found the field of Engineering very interesting. Saw the article Designing versatile sulfoximine as accepting unit to regulate the photophysical properties of TADF emitters towards high-performance OLEDs published in 2020, Reprint Addresses Yang, CL (corresponding author), Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Key Lab Polymer Sci & Technol, Shenzhen 518060, Peoples R China.. The CAS is 93-97-0. Through research, I have a further understanding and discovery of Benzoic anhydride.

This contribution describes sulfoximine (SFI) derivatives as a novel type of acceptor for efficient thermally activated delayed fluorescence (TADF) emitters. SFI presents a unique advantage by facile introduction of versatile functionalities on its secondary amine, which allows delicate manipulation of TADF properties. In a proof of principle study, three green/yellowish green TADF emitters, namely DMAC-SFIP, DMAC-SFIC and DMAC-SFIS were developed with different electron-withdrawing N-substituents based on simple donor-acceptor (D-A) typed structure. A look into the molecular conformations indicates the existence of different types of weak intramolecular interactions to suppress nonradiative decay. More importantly, effective mixing between charge transfer (CT) and locally excited (LE) triplet states is observed for DMAC-SFIP, DMAC-SFIC due to suitable electron-deficiency in the SFI segment, resulting in acceleration of the reverse intersystem crossing (RISC) rate. Consequently, these new TADF emitters render excellent organic light-emitting diode (OLED) performances with external quantum efficiencies (EQEs) up to 20.4% and small efficiency roll-off.

Application In Synthesis of Benzoic anhydride. About Benzoic anhydride, If you have any questions, you can contact Cao, XS; Chen, ZX; Gong, SL; Pan, K; Zhou, CJ; Huang, T; Chai, DY; Zhan, Q; Li, NQ; Zou, Y; Liu, H; Yang, CL or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

What about chemistry interests you the most 3-Methylbenzoic acid

About 3-Methylbenzoic acid, If you have any questions, you can contact Li, JY; Miklossy, G; Modukuri, RK; Bohren, KM; Yu, ZF; Palaniappan, M; Faver, JC; Riehle, K; Matzuk, MM; Simmons, N or concate me.. Formula: C8H8O2

In 2019.0 BIOCONJUGATE CHEM published article about SOLUBLE EPOXIDE HYDROLASE; COUPLING REACTIONS; SELECTION METHODS; SUZUKI-MIYAURA; ARYL HALIDES; INHIBITORS; OPTIMIZATION; EFFICIENT; LIGANDS; SYSTEM in [Li, Jian-Yuan; Miklossy, Gabriella; Modukuri, Ram K.; Bohren, Kurt M.; Yu, Zhifeng; Palaniappan, Murugesan; Faver, John C.; Riehle, Kevin; Matzuk, Martin M.; Simmons, Nicholas] Baylor Coll Med, Ctr Drug Discovery, Dept Pathol & Immunol, Houston, TX 77030 USA in 2019.0, Cited 50.0. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7. Formula: C8H8O2

A strategy for DNA-compatible, palladium-catalyzed hydroxycarbonylation of (hetero)aryl halides on DNA-chemical conjugates has been developed. This method generally provided the corresponding carboxylic acids in moderate to very good conversions for (hetero)aryl iodides and bromides, and in poor to moderate conversions for (hetero)aryl chlorides. These conditions were further validated by application within a DNA-encoded chemical library synthesis and subsequent discovery of enriched features from the library in selection experiments against two protein targets.

About 3-Methylbenzoic acid, If you have any questions, you can contact Li, JY; Miklossy, G; Modukuri, RK; Bohren, KM; Yu, ZF; Palaniappan, M; Faver, JC; Riehle, K; Matzuk, MM; Simmons, N or concate me.. Formula: C8H8O2

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

What about chemistry interests you the most C8H10O2

About 1,3-Dimethoxybenzene, If you have any questions, you can contact Mishiro, K; Nomura, M; Furuyama, T; Kunishima, M or concate me.. Quality Control of 1,3-Dimethoxybenzene

Quality Control of 1,3-Dimethoxybenzene. Authors Mishiro, K; Nomura, M; Furuyama, T; Kunishima, M in AMER CHEMICAL SOC published article about in [Nomura, Mitsuki; Kunishima, Munetaka] Kanazawa Univ, Fac Pharmaceut Sci, Inst Med Pharmaceut & Hlth Sci, Kanazawa, Ishikawa 9201192, Japan; [Furuyama, Taniyuki] Kanazawa Univ, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201192, Japan; [Furuyama, Taniyuki] Japan Sci & Technol Agcy JST PRESTO, Kawaguchi, Saitama 3320012, Japan; [Mishiro, Kenji] Kanazawa Univ, Inst Frontier Sci Initiat, Kanazawa, Ishikawa 9201192, Japan in 2021, Cited 37. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0

To improve the efficiency of the photocatalytic decarbonylation of cyclopropenones, the effects of substituents on cyclopropenone were explored. A benzothiophene-substituted aminocyclopropenone exhibited significantly improved decarbonylation efficiency to produce the corresponding ynamine, which worked as a potent dehydration condensation agent. The benzothiophene derivative was applicable to the photocatalytic reaction in the presence of potential excited-state quenchers such as oxygen and anilines. The high catalyst sensitivity would be attributed to the involvement of triplet energy transfer reaction pathway, which was not observed in the reaction with previously reported aminocyclopropenones.

About 1,3-Dimethoxybenzene, If you have any questions, you can contact Mishiro, K; Nomura, M; Furuyama, T; Kunishima, M or concate me.. Quality Control of 1,3-Dimethoxybenzene

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

What I Wish Everyone Knew About 2,6-Difluorobenzoic acid

SDS of cas: 385-00-2. About 2,6-Difluorobenzoic acid, If you have any questions, you can contact Madikizela, B; Eckhardt, T; Goddard, R; Richter, A; Lins, A; Lehmann, C; Imming, P; Seidel, RW or concate me.

SDS of cas: 385-00-2. I found the field of Pharmacology & Pharmacy very interesting. Saw the article Synthesis, structural characterization and antimycobacterial evaluation of several halogenated non-nitro benzothiazinones published in 2021, Reprint Addresses Seidel, RW (corresponding author), Martin Luther Univ Halle Wittenberg, Inst Pharm, Wolfgang Langenbeck Str 4, D-06120 Halle, Saale, Germany.. The CAS is 385-00-2. Through research, I have a further understanding and discovery of 2,6-Difluorobenzoic acid.

8-Nitro-1,3-benzothiazin-4-ones (BTZs), with BTZ043 and PBTZ169 as the most advanced compounds, represent a new class of potent antitubercular agents, which irreversibly inhibit decaprenylphosphoryl-beta-d-ribose-2 ‘-epimerase (DprE1), an enzyme crucial for cell wall synthesis in the pathogen Mycobacterium tuberculosis. Synthesis, structural characterization and in vitro testing against Mycobacterium aurum DSM 43999 and M. tuberculosis H(37)Rv of halogenated 2-(4-ethoxycarbonylpiperazin-1-yl)-1,3-benzothiazin-4-ones lacking a nitro group are reported. X-ray crystallography reveals that the structure of the BTZ scaffold can significantly deviate from planarity. In contrast to recent reports, the results of the present study indicate that further investigation of halogenated non-nitro BTZs for antitubercular activity is less than a promising approach.

SDS of cas: 385-00-2. About 2,6-Difluorobenzoic acid, If you have any questions, you can contact Madikizela, B; Eckhardt, T; Goddard, R; Richter, A; Lins, A; Lehmann, C; Imming, P; Seidel, RW or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Why do aromatic interactions matter of compound:93-02-7

COA of Formula: C9H10O3. About 2,5-Dimethoxybenzaldehyde, If you have any questions, you can contact Shaikh, S; Pavale, G; Dhavan, P; Singh, P; Uparkar, J; Vaidya, SP; Jadhav, BL; Ramana, MMV or concate me.

Authors Shaikh, S; Pavale, G; Dhavan, P; Singh, P; Uparkar, J; Vaidya, SP; Jadhav, BL; Ramana, MMV in ACADEMIC PRESS INC ELSEVIER SCIENCE published article about INDOLE-DERIVATIVES; BIOLOGICAL EVALUATION; ACETYLCHOLINESTERASE; AGENTS; ANTIOXIDANT; RAT in [Shaikh, Sarfaraz; Pavale, Ganesh; Uparkar, Jasmin; Ramana, M. M., V] Univ Mumbai, Dept Chem, Santacruz E, Mumbai 400098, Maharashtra, India; [Dhavan, Pratik; Jadhav, B. L.] Univ Mumbai, Dept Life Sci, Santacruz E, Mumbai 400098, Maharashtra, India; [Singh, Pinky; Vaidya, S. P.] Haffkine Inst, Dept Microbiol, Mumbai 400012, Maharashtra, India in 2021, Cited 41. COA of Formula: C9H10O3. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7

A series of novel dihydropyranoindole derivatives containing sulphonamide group were designed, synthesized and evaluated for in-vitro anti-cholinesterase activity. The result showed that all the compounds exhibited potent acetylcholinesterase (AChE) activity (IC50 = 0.41-8.79 mu M) while demonstrated moderate to good activity for butyrylcholinesterase (BuChE) (IC50 = 1.17-30.17 mu M). The tested compounds exhibited selectivity towards AChE over BuChE. Compound 5o was most potent towards both AChE (IC50 = 0.41 mu M) and BuChE (IC50 = 1.17 mu M) when compared to standard galantamine and rivastigmine. Enzyme kinetics and molecular docking studies revealed that compound 5o shows mixed type inhibition and binds to peripheral anionic site (PAS) and the catalytic sites (CAS) of both the enzymes. Furthermore, cell viability studies were also performed against N2a cells along with neuroprotection studies against H2O2 in the same cell line. Antioxidant studies using DPPH radical and H2O2 were also performed which revealed that all compounds possessed some antioxidant activity. Also, DNA damage protection assay for compound 5o was performed implying that compound 5o was protective in nature. ADME studies were also performed which demonstrated good pharmacokinetics. These findings indicated that dihydropyranoindole derivatives could be possible drug lead in the search for new multifunctional AD drugs.

COA of Formula: C9H10O3. About 2,5-Dimethoxybenzaldehyde, If you have any questions, you can contact Shaikh, S; Pavale, G; Dhavan, P; Singh, P; Uparkar, J; Vaidya, SP; Jadhav, BL; Ramana, MMV or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Final Thoughts on Chemistry for 99-04-7

About 3-Methylbenzoic acid, If you have any questions, you can contact Jette, CI; Tong, ZJ; Hadt, RG; Stoltz, BM or concate me.. HPLC of Formula: C8H8O2

Recently I am researching about ASYMMETRIC-SYNTHESIS; CONJUGATE ADDITION; ALDOL ADDITIONS; COMPLEXES; LACTONES; REGIOSELECTIVITY; SUBSTITUTION; MECHANISM; BOND, Saw an article supported by the NIH-NIGMSUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USANIH National Institute of General Medical Sciences (NIGMS) [R01GM080269]; Caltech; Dow Next Generation Educator Fund; National Science FoundationNational Science Foundation (NSF). Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Jette, CI; Tong, ZJ; Hadt, RG; Stoltz, BM. The CAS is 99-04-7. Through research, I have a further understanding and discovery of 3-Methylbenzoic acid. HPLC of Formula: C8H8O2

Herein, we report a Cu-catalyzed enantioselective allylic alkylation using a gamma-butyrolactone-derived silyl ketene acetal. Critical to the development of this work was the identification of a novel mono-picolinamide ligand with the appropriate steric and electronic properties to afford the desired products in high yield (up to 96 %) and high ee (up to 95 %). Aryl, aliphatic, and unsubstituted allylic chlorides bearing a broad range of functionality are well-tolerated. Spectroscopic studies reveal that a Cu-I species is likely the active catalyst, and DFT calculations suggest ligand sterics play an important role in determining Cu coordination and thus catalyst geometry.

About 3-Methylbenzoic acid, If you have any questions, you can contact Jette, CI; Tong, ZJ; Hadt, RG; Stoltz, BM or concate me.. HPLC of Formula: C8H8O2

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Something interesting about 93-02-7

About 2,5-Dimethoxybenzaldehyde, If you have any questions, you can contact Gur, M; Yerlikaya, S; Sener, N; Ozkinali, S; Baloglu, MC; Gokce, H; Altunoglu, YC; Demir, S; Sener, I or concate me.. SDS of cas: 93-02-7

An article Antiproliferative-antimicrobial properties and structural analysis of newly synthesized Schiff bases derived from some 1,3,4-thiadiazole compounds WOS:000569381800011 published article about ANTITUMOR-ACTIVITY; CELL-LINE; DERIVATIVES; ANTICANCER; PC3; INHIBITION; COMPLEXES; APOPTOSIS; DOCKING; NI(II) in [Gur, Mahmut] Kastamonu Univ, Dept Forest Ind Engn, Kastamonu, Turkey; [Yerlikaya, Serife; Baloglu, Mehmet Cengiz; Altunoglu, Yasemin Celik] Kastamonu Univ, Dept Genet & Bioengn, Kastamonu, Turkey; [Sener, Nesrin] Kastamonu Univ, Dept Chem, Kastamonu, Turkey; [Ozkinali, Sevil] Hitit Univ, Dept Chem, Corum, Turkey; [Baloglu, Mehmet Cengiz] Univ Florida, IFAS, Dept Agron, Gainesville, FL 32611 USA; [Gokce, Halil] Giresun Univ, Vocat Sch Hlth Serv, Giresun, Turkey; [Demir, Serkan] Giresun Univ, Dept Ind Engn, Giresun, Turkey; [Sener, Izzet] Kastamonu Univ, Dept Food Engn, Kastamonu, Turkey in 2020.0, Cited 69.0. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7. SDS of cas: 93-02-7

The 1,3,4-thiadiazole core has been mainly used as a pharmacological scaffold in medicinal chemistry. A series of Schiff bases derived from 5-substituted-1,3,4-thiadiazole-2-amine were designed and synthesized to investigate their biological activities. Structures of compounds were clarified with FTIR, H-1 NMR and elemental analysis. Due to the importance of this core in pharmacology, all these newly synthesized compounds were tested for different biological properties at the same time. Compound 3A ((E)-N-(2,5-dimethoxybenzylidene)-5-(4-methoxyquinolin-2-yl)-1,3,4-thiadiazol-2-amine) and compound 4A ((E)-N-(2,5-dimethoxybenzylidene)-5-(3-methylbenzofuran-2-yl)-1,3,4-thiadiazol-2-amine) possessed high DNA protective ability against oxidative Fenton mixture. Compound 1A ((E)-N-(2,5-dimethoxybenzylidene)-5-(benzo[b]thiophen-2-yl)-1,3,4-thiadiazol-2-amine) and compound 2B ((E)-2-((5-(1H-indol-2-yl)-1,3,4-thiadiazol-2-ylimino)methyl)-6-methoxyphenol) showed strong antimicrobial activity against S. epidermidis. The most effective compound was detected as compound 3A which exhibited cytotoxicity on both PC-3 and MDA-MB-231 cancer cell lines. The IC50 of this compound was calculated as 370.7 mu M and 505.1 mu M for MDA-MB-231 and PC-3 cells, respectively. Molecular docking studies were also performed to examine the understanding of the mechanism behind the anti-cancer and anti-bacterial properties. For further study, compound 3A has the potential for utilization with chemotherapy drugs to establish a more efficient therapy strategy with minimum cytotoxicity against cancer cells. (C) 2020 Elsevier B.V. All rights reserved.

About 2,5-Dimethoxybenzaldehyde, If you have any questions, you can contact Gur, M; Yerlikaya, S; Sener, N; Ozkinali, S; Baloglu, MC; Gokce, H; Altunoglu, YC; Demir, S; Sener, I or concate me.. SDS of cas: 93-02-7

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Simple exploration of 1,3-Dimethoxybenzene

Category: isothiazole. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Singh, SK; Dhepe, PL or concate me.

In 2019 IND ENG CHEM RES published article about REDISTRIBUTION MECHANISM; DEPOLYMERIZATION; BIOMASS; WATER; VALORIZATION; LIQUEFACTION; CHEMICALS; BIOFUELS; SOLVENTS; HYDROLYSIS in [Singh, Sandip K.; Dhepe, Paresh L.] Natl Chem Lab, CSIR, Catalysis & Inorgan Chem Div, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India; [Singh, Sandip K.; Dhepe, Paresh L.] Acad Sci & Innovat Res AcSIR, New Delhi 110025, Uttar Pradesh, India in 2019, Cited 66. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. Category: isothiazole

Because it is undisputable that lignin depolymerization is a must to make the biorefinery concept economically feasible, several efforts are put toward it; however, a lot of catalyst designing is required to achieve efficient depolymerization activities. In this work, we show a systematic approach in the synthesis and characterization of ionic liquids (ILs) with varying combinations of cations (imidazole, benzimidazole, phosphonium, and ammonium) and anions (HSO4, PTS (p-toluenesulfonate), Cl, H2PO4, SnCl3, FeCl4, and CuCl3) for the depolymerization of lignin into low-molecular weight aromatic fractions (<220 g/mol) under mild reaction conditions (120 degrees C, 1 h, ambient pressure). In a methodical approach, effects of various reaction parameters such as temperature (70-170 degrees C), time (15-360 min), pressure (N-2, 0.5-3 MPa), solvents and substrate, and so forth were studied to achieve best activity. Among all the catalysts, IL with the imidazolium cation and HSO4 as the anion showed best activity (78% yield). Subsequent to depolymerization, three aromatic monomers (5 wt % pure vanillin) were isolated using flash column chromatography. These aromatic monomers were characterized using gas chromatography (GC), GC-mass spectrometry, and NMR techniques for their purity. Hammett acidity functions (H-0) of ILs were measured using UV-vis photo-spectroscopy, and values are correlated with lignin depolymerization results. Lignin and tetrahydrofuran-soluble products were thoroughly characterized using assorted physicochemical techniques such as NMR (H-1 and C-13), gel permittivity chromatography, thermogravimetric analysis, and so forth. The catalyst was recycled up to six runs and showed similar results in consecutive reactions. Category: isothiazole. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Singh, SK; Dhepe, PL or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Get Up to Speed Quickly on Emerging Topics:3-Methylbenzoic acid

Recommanded Product: 3-Methylbenzoic acid. About 3-Methylbenzoic acid, If you have any questions, you can contact Zhou, X; Xu, HY; Yang, QD; Chen, H; Wang, SF; Zhao, HQ or concate me.

Recommanded Product: 3-Methylbenzoic acid. Zhou, X; Xu, HY; Yang, QD; Chen, H; Wang, SF; Zhao, HQ in [Zhou, Xi; Xu, Hongyan; Yang, Qiaodan; Chen, Hua; Zhao, Huaiqing] Univ Jinan, Sch Chem & Chem Engn, Jinan 250022, Shandong, Peoples R China; [Wang, Shoufeng] Univ Jinan, Shandong Prov Key Lab Fluorine Chem & Chem Mat, Sch Chem & Chem Engn, Jinan 250022, Shandong, Peoples R China published Co(ii)/Cu(ii)-cocatalyzed oxidative C-H/N-H functionalization of benzamides with ketones: a facile route to isoindolin-1-ones in 2019, Cited 64. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

A cobalt and copper catalyzed reaction protocol has been developed to achieve the oxidative C-H/N-H annulation of benzamides containing an 8-aminoquinoline moiety as the directing group with ketones. Structurally diverse isoindolin-1-ones were furnished by the reaction of various substituent benzamides with ketones.

Recommanded Product: 3-Methylbenzoic acid. About 3-Methylbenzoic acid, If you have any questions, you can contact Zhou, X; Xu, HY; Yang, QD; Chen, H; Wang, SF; Zhao, HQ or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Search for chemical structures by a sketch :C7H4F2O2

Category: isothiazole. About 2,6-Difluorobenzoic acid, If you have any questions, you can contact Liang, XL; Radosevich, M; Loffler, F; Schaeffer, SM; Zhuang, J or concate me.

Category: isothiazole. Recently I am researching about COLLOID TRANSPORT; SILVER NANOPARTICLES; ANAEROBIC BIOREMEDIATION; MINERALIZATION PATHWAYS; FLOW CONDITIONS; ORGANIC-MATTER; POROUS-MEDIA; HEAVY-METALS; MOBILIZATION; TRANSFORMATION, Saw an article supported by the United States Strategic Environmental Research and Development Program (SERDP) [ER-2130]; China Scholarship CouncilChina Scholarship Council. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Liang, XL; Radosevich, M; Loffler, F; Schaeffer, SM; Zhuang, J. The CAS is 385-00-2. Through research, I have a further understanding and discovery of 2,6-Difluorobenzoic acid

In subsurface bioremediation, electron donor addition promotes microbial Fe(lII)-oxide mineral reduction that could change soil pore structure, release colloids, and alter soil surface properties. These processes in turn may impact bioremediation rates and the ultimate fate of contaminants. Columns packed with water-stable, Fe-oxide-rich soil aggregates were infused with acetate-containing artificial groundwater and operated for 20 d or 60 d inside an anoxic chamber. Soluble Fe(II) and soil colloids were detected in the effluent within one week after initiation of the acetate addition, demonstrating Fe(III)-bioreduction and colloid formation. Diffusible Br-, less diffusible 2,6-difluorobenzoate (DFBA), and non-diffusible silica-shelled silver nanoparticles (SSSNP) were used as tracers in transport experiments before and after the bioreduction. The transport of Br- was not influenced by the bioreduction. DFBA showed earlier breakthrough and less tailing after the bioreduction, suggesting alterations in flow paths and soil surface chemistry during the 20-d bioreduction treatment. Similarly, the bioreduction increased the transport of SSSNP very significantly, with mass recovery increasing from 1.7% to 25.1%. Unexpectedly, the SSSNP was completely retained in the columns when the acetate injection was extended from 20 to 60 d, while the mass recovery of DFBA decreased from 89.1% to 84.1% and Br showed no change. The large change in the transport of SSSNP was attributed to soil aggregate breakdown and colloid release (causing mechanical straining of SSSNP) and the exposure of iron oxide surfaces previously unavailable within aggregate interiors (facilitating attachment of SSSNP). These results suggest a time dependent fashion of microbial effect on the transport of diffusivity-varying tracers. (C) 2018 Elsevier Ltd. All rights reserved.

Category: isothiazole. About 2,6-Difluorobenzoic acid, If you have any questions, you can contact Liang, XL; Radosevich, M; Loffler, F; Schaeffer, SM; Zhuang, J or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com