1956-44-1 Usage
Description
(1E)-N-hydroxy-1-(5-methylthiophen-2-yl)ethanimine, also known as 5-methylthiophen-2-ylhydroximine, is an organic compound with the chemical formula C7H9NOS. It is an N-hydroxyimine derivative, which means it contains an N-hydroxy functional group (-NOH) attached to an imine functional group (C=N). Its unique structure and properties make it useful in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the presence of the thiophene ring in its structure gives it potential biological activity and makes it of interest for medicinal chemistry applications.
Uses
Used in Chemical Synthesis:
(1E)-N-hydroxy-1-(5-methylthiophen-2-yl)ethanimine is used as a reagent or intermediate in the production of various organic compounds. Its unique structure and properties make it useful in the development of pharmaceuticals, agrochemicals, and other fine chemicals.
Used in Medicinal Chemistry:
(1E)-N-hydroxy-1-(5-methylthiophen-2-yl)ethanimine is used as a compound of interest for medicinal chemistry applications due to its potential biological activity and the presence of the thiophene ring in its structure.
Check Digit Verification of cas no
The CAS Registry Mumber 1956-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1956-44:
(6*1)+(5*9)+(4*5)+(3*6)+(2*4)+(1*4)=101
101 % 10 = 1
So 1956-44-1 is a valid CAS Registry Number.
1956-44-1Relevant articles and documents
gem-DIALKOXYLATION OF 2-ACETYLTHIOPHENES AND 2-ACETYLFURANS
Gordeeva, G. N.,Kalashnikov, S. M.,Popov, Yu. N.,Kruglov, E. A.,Imashev, U. B.
, p. 638 - 641 (2007/10/02)
Reaction of 2-acetyl-substituted thiophenes and furans with alkyl nitrites in the presence of the corresponding aliphatic alcohols and hydrochloric acid leads to the formation of linear acetals of thienyl- and furylglyoxals, whose structure was established by IR, UV, NMR spectroscopy, and mass spectrometry methods.The main paths of the dissociation of the molecules under electron impact were established.
