37072-50-7 Usage
Molecular structure
Contains a thiazole ring and a benzylidenehydrazinyl group.
Synthesis
Derived from the reaction between 2-hydrazinothiazole and benzaldehyde.
Physical appearance
Yellowish solid.
Solubility
Slightly soluble in water, more soluble in organic solvents.
Potential applications
Pharmaceutical and chemical research.
Characteristics
Diverse chemical properties and biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 37072-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,7 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37072-50:
(7*3)+(6*7)+(5*0)+(4*7)+(3*2)+(2*5)+(1*0)=107
107 % 10 = 7
So 37072-50-7 is a valid CAS Registry Number.
37072-50-7Relevant academic research and scientific papers
Bromination of 4-Substituted Thiazolylhydrazones
Denisova, A. B.,Andronnikova, G. P.
, p. 863 - 867 (2007/10/03)
4-Phenyl- and 4-methylthiazolylhydrazones were brominated in chloroform and acetic acid.The use of 1.5 equivalents of bromine led to the exclusive formation of the 5-halo derivatives.Effects of substituents on the thiazole ring and of the hydrazone fragme
Nitrosation and Hydrolysis Studies of some Thiazole-4-acetic Esters
Campaigne, E.,Selby, T. P.
, p. 1249 - 1253 (2007/10/02)
Nitrosation of hydrazino substituted thiazole-4-acetates has been shown to occur on the ring, rather than the α-methylene carbon, as previously reported.Thus nitrosation of ethyl 2-isopropylidenehydrazono-, 2-benzylidenehydrazono-, 2-(2-benzoylhydrazino)-
