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2-Hydroxymethyl-4-methylimidazole is an organic compound with the chemical formula C5H8N2O. It is a derivative of imidazole, a heterocyclic aromatic organic compound containing two nitrogen atoms in its ring structure. This specific compound features a methyl group (-CH3) attached to the 4th carbon of the imidazole ring and a hydroxymethyl group (-CH2OH) attached to the 2nd carbon. 2-Hydroxymethyl-4-methylimidazole is a colorless solid with a melting point of approximately 65-67°C. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its reactivity, it is typically handled under controlled conditions to prevent unwanted side reactions or degradation.

872-79-7

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872-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872-79-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 872-79:
(5*8)+(4*7)+(3*2)+(2*7)+(1*9)=97
97 % 10 = 7
So 872-79-7 is a valid CAS Registry Number.

872-79-7Downstream Products

872-79-7Relevant academic research and scientific papers

Monocyclic, substituted imidazoles as glycosidase inhibitors

Magdolen, Peter,Vasella, Andrea

, p. 2454 - 2469 (2007/10/03)

A range of 4-monosubstituted and 2,4-disubstituted 1H-imidazoles and 1H-imidazole-1-ethanols (R-C(4): CH2CH2Ph, CHOHCH 2Ph, Ph, or Me; R-C(2): CH2OH, CHOHCH2OH, CN, or CH2NHAc) were prepare

SYNTHESIS OF A CIMETIDINE ANALOGUE

Heiszman, Jozsef,Harsanyi, Kalman,Toke, Laszlo

, p. 2487 - 2491 (2007/10/02)

2-Hydroxymethyl-4-methylimidazole (2a) and 2,5-bis(hydroxymethyl)-4-methylimidazole (3a) have been synthesized and characterized.No reaction on the hydroxymethyl moieties in position 2 of these compounds could be observed with cysteamine under usual reaction conditions.The hydroxymethyl group in position 5 of compound 3a does react with cysteamine to give an intermediate leading to 3b and to cimetidine analogue 3c.

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