61982-14-7

Basic information

• Product Name: 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI)
• Synonyms: 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI);1-methyl-4-nitroimidazole-5-carboxylic acid chloride
• CAS NO: 61982-14-7
• Molecular Formula: C₅H₄ClN₃O₃
• Molecular Weight: 189.558
• Product Categories: ACIDHALIDE
• Mol File: 61982-14-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 409.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.70±0.1 g/cm3(Predicted)
• PKA: -3.67±0.61(Predicted)
• CAS DataBase Reference: 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI)(61982-14-7)
• EPA Substance Registry System: 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI)(61982-14-7)

Safety Data

• Hazardous Substances Data: 61982-14-7(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline solid The compound is a yellow solid with a crystalline structure.

Molecular weight

198.58 g/mol The molecular weight of the compound is approximately 198.58 grams per mole.

Derivative

Carbonylchloride derivative of 1-methyl-4-nitroimidazole 1H-Imidazole-5-carbonylchloride,1-methyl-4-nitro-(9CI) is derived from 1-methyl-4-nitroimidazole by the addition of a carbonylchloride group.

Usage

Organic synthesis and pharmaceutical research The compound is commonly used as a building block in the synthesis of various heterocyclic compounds and pharmaceutical intermediates.

Structural features

Imidazole and nitro groups The presence of both imidazole and nitro groups in the structure makes the compound versatile for various chemical reactions and applications.

Toxicity

Likely toxic The compound is potentially toxic, and proper safety measures should be taken when handling it in the laboratory.

Upstream product

• 54828-05-6 1-methyl-4-nitro-1H-imidazole-5-carboxylic acid 
• 5413-88-7 5-Carboxamido-1-methyl-4-nitroimidazole 
• 40648-96-2 1-methyl-4-nitro-1H-imidazole-5-carbonitrile 

Downstream Products

• 132038-66-5 3-methyl-5-nitro-3H-imidazole-4-carboxylic acid-(2-hydroxy-ethylamide) 
• 223123-49-7 1-methyl-5-phenyl-7-oxo-4,7-dihydro-1H-imidazo<4,5-b>pyridine-6-carboxylic acid 
• 223123-27-1 ethyl 1-methyl-5-phenyl-7-oxo-4,7-dihydro-1H-imidazo<4,5-b>pyridine-6-carboxylate 
• 223122-99-4 ethyl 4-hydroxy-1-methyl-5-phenyl-7-oxo-4,7-dihydro-1H-imidazo<4,5-b>pyridine-6-carboxylate 
• 611-59-6 paraxanthine 
• 61982-18-1 4-amino-1-methylimidazole-5-carboxylate ethyl ester 
• 858221-03-1 5-amino-3-methyl-3H-imidazole-4-carboxylic acid methylamide 

Relevant articles and documents

Synthesis of 2-hydroxyethyl and 2-chloroethyl esters of 1-alkyl (1,2-dialkyl)-4-Aminoimidazolyl-5-carboxylic acids

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SULFONAMIDE DERIVATIVE AND MEDICINAL USE THEREOF

Provided are sulfonamide derivatives of a specific chemical structure in which a sulfonamide group having, as a substituent, a phenyl group or a heterocyclic group having a hetero atom(s) as a constituent element(s) is present at its terminal, and pharmaceutically acceptable salts thereof. These compounds are novel compounds having excellent α4 integrin-inhibitory action.

Synthesis of 2-hydroxy- and 2-diethylamino-ethylamides of 1-alkyl(1,2-dialkyl)-4-aminoimidazolyl-5-carboxylic acids

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