71226-51-2 Usage
Structure
2-(methylsulfanyl)-5-(4-nitrophenyl)-1,3-thiazol-4-amine has a thiazole ring structure, with a methylsulfanyl group attached to the second carbon of the ring and a nitrophenyl group attached to the fifth carbon.
Biological activity
2-(methylsulfanyl)-5-(4-nitrophenyl)-1,3-thiazol-4-amine has potential biological activities, which means it may have effects on living organisms.
Research applications
The compound may be used in research related to drug development and therapeutic treatments, indicating its potential as a pharmaceutical agent.
Handling precautions
2-(methylsulfanyl)-5-(4-nitrophenyl)-1,3-thiazol-4-amine should be handled with care due to its potential to be hazardous if not properly stored and managed.
Check Digit Verification of cas no
The CAS Registry Mumber 71226-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71226-51:
(7*7)+(6*1)+(5*2)+(4*2)+(3*6)+(2*5)+(1*1)=102
102 % 10 = 2
So 71226-51-2 is a valid CAS Registry Number.
71226-51-2Relevant articles and documents
SYNTHESIS AND PROPERTIES OF 4-AMINO-5-(5-X-2-FURYL)THIAZOLE DERIVATIVES
Krapivin, Gennadii D.,Jurasek, Adolf,Kovac, Jaroslav,Kul'nevich, Vladimir G.
, p. 2285 - 2294 (2007/10/02)
Reaction of dipotassium cyanimidodithiocarbonate ((KS)2C=N-CN) with 5-X-furfuryl halogenides (X=NO2, CHO) and 4-nitrobenzyl bromide gives the disubstituted esters which, in alkali medium, gives the carbanions undergoing cyclization to 4-amino-5-(5-X-2-fur
