4897-31-8 Usage
Description
4-Chloro-1-methyl-5-nitro-1H-imidazole is a chemical compound with the molecular formula C4H4ClN3O2. It is a derivative of imidazole with a chlorine atom at the 4 position and a nitro group at the 5 position. This yellow solid has a molecular weight of 155.55 g/mol and is soluble in organic solvents such as acetone and methanol. Due to its potential harmful effects if swallowed, inhaled, or in contact with the skin, it is important to handle this compound with caution.
Uses
Used in Organic Synthesis:
4-Chloro-1-methyl-5-nitro-1H-imidazole is used as a building block in the preparation of various pharmaceuticals and agrochemicals. Its unique structure allows it to be a versatile component in the synthesis of a wide range of compounds.
Used as a Reagent:
In the field of organic chemistry, 4-CHLORO-1-METHYL-5-NITRO-1H-IMIDAZOLE also serves as a reagent in the synthesis of other organic compounds. Its presence can facilitate or enhance the reactions required to produce desired end products, making it a valuable asset in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 4897-31-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4897-31:
(6*4)+(5*8)+(4*9)+(3*7)+(2*3)+(1*1)=128
128 % 10 = 8
So 4897-31-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H4ClN3O2/c1-7-2-6-3(5)4(7)8(9)10/h2H,1H3
4897-31-8Relevant articles and documents
A New and Unequivocal Method for Establishing the Position of N-Glycosylation of Unsymmetrically C-Substituted Imidazoles
Benson, Timothy J.,Robinson, Brian
, p. 211 - 214 (2007/10/02)
N-Substitution of an unsymmetrically C-substituted imidazole can give rise to a pair of structurally isomeric derivatives and to differentiate between such related compounds can be difficult.Two methods, one spectroscopic and one chemical, for ascertaining the orientation of such N-substitutions are described, with particular application to the establishment of the direction of N-ribosidation of a series of halogeno nitroimidazoles.
