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4022-89-3

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4022-89-3 Usage

General Description

1-METHYL-5-(METHYLAMINO)-1H-IMIDAZOLE-4-CARBOXAMIDE is a chemical compound with the molecular formula C7H10N4O. It is an imidazole derivative with a carboxamide group, and the methyl and methylamino substituents on the 1 and 5 positions of the imidazole ring, respectively. 1-METHYL-5-(METHYLAMINO)-1H-IMIDAZOLE-4-CARBOXAMIDE has potential pharmaceutical applications, particularly in the development of new drugs and medications. It may also be used as a research tool for studying biological processes and chemical reactions. The precise properties and uses of 1-METHYL-5-(METHYLAMINO)-1H-IMIDAZOLE-4-CARBOXAMIDE are still under investigation, and further research is needed to fully understand its potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4022-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4022-89:
(6*4)+(5*0)+(4*2)+(3*2)+(2*8)+(1*9)=63
63 % 10 = 3
So 4022-89-3 is a valid CAS Registry Number.

4022-89-3Upstream product

4022-89-3Relevant articles and documents

SYNTHESIS OF 3,9-DIALKYLGUANINES AND THEIR CONVERSION INTO 3-ALKYLWYES, MODELS FOR THE FLUORESCENT NUCLEOSIDES FROM PHENYLALANINE TRANSFER RIBONUCLEIC ACIDS

Itaya, Taisuke,Ogawa, Kazuo

, p. 1767 - 1774 (2007/10/02)

Synthesis of 3,9-dialkylguanines 5 has been accomplished by N-cyanation of 1-alkyl-5-(alkylamino)imidazole-4-carboxamides 3 followed by base-catalysed cyclisation.Cyclocondensation of 9-alkyl-3-methylguanines 5a, d, f with MeCOCH2Br gave 3-alkylwyes 6, model compounds of the most probable structure for wyosine from Torulopsis utilis tRNAPhe.

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