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1-Methyl-5-(methylamino)-1H-imidazole-4-carboxamide, also known as Midazolam, is a short-acting benzodiazepine with sedative, hypnotic, anxiolytic, muscle relaxant, and amnesic properties. It is commonly used in medical procedures for its sedative and amnestic effects, as well as for the treatment of insomnia and anxiety disorders. The chemical structure consists of an imidazole ring with a methyl group at the 1-position, a methylamino group at the 5-position, and a carboxamide group at the 4-position. Midazolam is water-soluble and has a rapid onset of action, making it a popular choice for medical professionals. However, it is important to note that it has a potential for abuse and dependence, and its use should be carefully monitored.

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 academic research and scientific papers

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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