184881-74-1

Basic information

• Product Name: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)thioxomethyl]amino]sulfonyl][ 1,1'-biphenyl]-4-yl]methyl]-, ethyl ester
• CAS NO: 184881-74-1
• Molecular Formula: C28H36N4O4S3
• Molecular Weight: 588.816
• Mol File: 184881-74-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)thioxomethyl]amino]sulfonyl][ 1,1'-biphenyl]-4-yl]methyl]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)thioxomethyl]amino]sulfonyl][ 1,1'-biphenyl]-4-yl]methyl]-, ethyl ester(184881-74-1)
• EPA Substance Registry System: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)thioxomethyl]amino]sulfonyl][ 1,1'-biphenyl]-4-yl]methyl]-, ethyl ester(184881-74-1)

Safety Data

• Hazardous Substances Data: 184881-74-1(Hazardous Substances Data)

Usage

Imidazole ring

The compound contains a 5-membered imidazole ring, which is an aromatic heterocyclic ring with 2 nitrogen atoms.

Carboxylic acid group

The compound has a carboxylic acid group (-COOH) attached to the imidazole ring, which is known for its acidic properties.

Butyl and methylthio groups

The compound has a butyl (C4H9) and a methylthio (CH3S) group attached to the imidazole ring, which contribute to its lipophilicity and steric properties.

Sulfonamide group

The compound features a sulfonamide group (-SO2NH2), which is a common functional group in pharmaceuticals and can act as a hydrogen bond acceptor.

Biphenyl moiety

The compound contains a biphenyl group (C6H5-C6H5), which is known for its rigidity and planarity, and can contribute to the compound's structure and activity.

Ethyl ester functional group

The compound has an ethyl ester (-COOCH2CH3) group, which can affect the compound's solubility and reactivity.

Pharmaceutical or industrial applications

Due to its complex structure and diverse functional groups, the compound may have potential applications in the pharmaceutical or industrial sectors, although further research would be needed to confirm its activity or reactivity in specific contexts.

Upstream product

• 628-30-8 n-Propyl isothiocyanate 
• 144629-51-6 ethyl 1-<<2'-(aminosulfonyl)(1,1'-biphenyl)-4-yl>methyl>-2-butyl-4-(methylthio)-1H-imidazole-5-carboxylate 
• 32683-02-6 ethyl-2-aminocyano acetate 
• 144629-50-5 ethyl 3-amino-3-(methylthio)-2-<(1-oxopentyl)amino>-2-propenoate 
• 137997-30-9 ethyl 2-n-butyl-4-(methylthio)-1H-imidazole-5-carboxylate 
• 139742-83-9 ethyl 2-cyano-2-n-butylcarbonylaminoacetate 
• 638-29-9 n-valeryl chloride 
• 92748-09-9 2-bromobenzene-1-sulfonamide 
• 5720-05-8 4-methylphenylboronic acid 

Downstream Products

• 144628-51-3 ethyl 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)-carbonyl]-amino]-sulfonyl]-(1,1'-biphenyl)-4-yl]-methyl]-1H-imidazole-5-carboxylate 
• 184881-75-2 2-Butyl-5-methylsulfanyl-3-(2'-{[1-methylsulfanyl-1-propylamino-meth-(Z)-ylidene]-sulfamoyl}-biphenyl-4-ylmethyl)-3H-imidazole-4-carboxylic acid ethyl ester 

Relevant articles and documents

Efficient two-step synthesis of sulfonylguanidines from sulfonamides

Various sulfonylguanidines have been synthesized from a sulfonamide by two mild and efficient synthetic methods. In route A, the methylthio group of S-methylsulfonylisothiourea is displaced by a variety of amines while in route B the amines are reacted wi