A new application about C7H7FO

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 459-56-3. Computed Properties of C7H7FO.

Chemistry, like all the natural sciences, Computed Properties of C7H7FO, begins with the direct observation of nature¡ª in this case, of matter.459-56-3, Name is (4-Fluorophenyl)methanol, SMILES is OCC1=CC=C(F)C=C1, belongs to isothiazole compound. In a document, author is Abd El-Nabi, HA, introduce the new discover.

1-aryl-5-methoxypyrrolones as synthons for fused heterocycles

3-Di(methylsulfonyl)methylene-pyrrol-2-one and 2-(1-aryl-5-methoxy-2-oxo-2,3-dihydro-1H-3-pyrrolylidene)malononitrile were obtained from 1-aryl-5-methoxypyrrolones. Aziridine and hydroxylamine reacted with pyrrol-2-one to afford 2,7-diazaspiro[4.4]-nona-3,6-diene and oxime derivatives, respectively. Pyrrolo[2,3-c]isoxazoles or pyrrolo[2,3-c]isothiazole were formed in high yield from oximes depending upon the reaction conditions employed for ring closure. Treatment of pyrrolylidene malononitrile with N-1,N-2-di(4-chlorophenyl)acetamidine in ethyl acetate furnished azepine derivatives in 70-75% yield. (C) 2002 Elsevier Science Ltd. All rights reserved.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 459-56-3. Computed Properties of C7H7FO.

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