Category: 3912-37-6

3912-37-6, Name is Isothiazole-4-carbonitrile, belongs to isothiazole compound, is a common compound. HPLC of Formula: C4H2N2SIn an article, once mentioned the new application about 3912-37-6.

The in situ Generation of Thiazyl Trichloride: A Synthon for C-N-S Heterocycles

The novel reagent NSCl3 is readily generated by treatment of (NSCl)3 with an excess of SO2Cl2; the reactions of NSCl3 with methacrylonitrile or thioacetamide produce 4-cyanoisothiazole or 5-methyl-1,3,2,4-dithiazolium chloride, respectively, in good yields.

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Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. COA of Formula: C4H2N2S, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 3912-37-6, name is Isothiazole-4-carbonitrile. In an article£¬Which mentioned a new discovery about 3912-37-6

Synthetic applications and spectroscopic investigations of the (NSCl)3-SO2Cl2 system

Solutions of (NSCl)3 in the presence of excess SO2Cl2 behave as a source of the synthetic equivalent “NSCl3” in reactions with methacrylonitrile or thioacetamide to give 4-cyanoisothiazole (78percent) or 5-methyl-1,3,2,4-dithiadiazolium chloride (63percent), respectively.In the reaction of this reagent with thiobenzamide both 5-phenyl-1,3,2,4-dithiadiazolium chloride (42percent) and 3,5-diphenyl-1,2,4-thiadiazole (51percent) are produced.The treatment of the (NSCl)3-SO2Cl2 system with 2-aminobenzenethiol yields 2,4-C6H3Cl2NSCl2, which is converted to 2,4-(C6H3Cl2N)2S upon heating at 80 deg C in toluene or by reduction with Ph3Sb or mercury.The reaction of 2-aminobenzenethiol with excess SO2Cl2, in the absence of (NSCl)3, produces 2,4,6-C6H2Cl3NSCl2.Attempts to characterize the active species in the (NSCl)3-SO2Cl2 system by 14N and 33S NMR, Raman and infrared spectroscopy are also described.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, COA of Formula: C4H2N2S, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 3912-37-6

Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of Isothiazole-4-carbonitrile, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 3912-37-6, Name is Isothiazole-4-carbonitrile, molecular formula is C4H2N2S

The in situ Generation of Thiazyl Trichloride: A Synthon for C-N-S Heterocycles

The novel reagent NSCl3 is readily generated by treatment of (NSCl)3 with an excess of SO2Cl2; the reactions of NSCl3 with methacrylonitrile or thioacetamide produce 4-cyanoisothiazole or 5-methyl-1,3,2,4-dithiazolium chloride, respectively, in good yields.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of Isothiazole-4-carbonitrile, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 3912-37-6

Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Product Details of 3912-37-6, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 3912-37-6, name is Isothiazole-4-carbonitrile. In an article£¬Which mentioned a new discovery about 3912-37-6

Synthetic applications and spectroscopic investigations of the (NSCl)3-SO2Cl2 system

Solutions of (NSCl)3 in the presence of excess SO2Cl2 behave as a source of the synthetic equivalent “NSCl3” in reactions with methacrylonitrile or thioacetamide to give 4-cyanoisothiazole (78percent) or 5-methyl-1,3,2,4-dithiadiazolium chloride (63percent), respectively.In the reaction of this reagent with thiobenzamide both 5-phenyl-1,3,2,4-dithiadiazolium chloride (42percent) and 3,5-diphenyl-1,2,4-thiadiazole (51percent) are produced.The treatment of the (NSCl)3-SO2Cl2 system with 2-aminobenzenethiol yields 2,4-C6H3Cl2NSCl2, which is converted to 2,4-(C6H3Cl2N)2S upon heating at 80 deg C in toluene or by reduction with Ph3Sb or mercury.The reaction of 2-aminobenzenethiol with excess SO2Cl2, in the absence of (NSCl)3, produces 2,4,6-C6H2Cl3NSCl2.Attempts to characterize the active species in the (NSCl)3-SO2Cl2 system by 14N and 33S NMR, Raman and infrared spectroscopy are also described.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 3912-37-6, help many people in the next few years.Product Details of 3912-37-6

Reference£º
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com