178979-44-7

Basic information

• Product Name: {5-[(3-chlorophenyl)sulfanyl]-4-(1-methylethyl)-1-propyl-1H-imidazol-2-yl}methyl carbamate
• CAS NO: 178979-44-7
• Molecular Formula: C₁₇H₂₂ClN₃O₂S
• Molecular Weight: 367.8935
• Mol File: 178979-44-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 551°C at 760 mmHg
• Flash Point: 287°C
• Density: 1.28g/cm³
• Vapor Pressure: 3.45E-12mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: {5-[(3-chlorophenyl)sulfanyl]-4-(1-methylethyl)-1-propyl-1H-imidazol-2-yl}methyl carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: {5-[(3-chlorophenyl)sulfanyl]-4-(1-methylethyl)-1-propyl-1H-imidazol-2-yl}methyl carbamate(178979-44-7)
• EPA Substance Registry System: {5-[(3-chlorophenyl)sulfanyl]-4-(1-methylethyl)-1-propyl-1H-imidazol-2-yl}methyl carbamate(178979-44-7)

Safety Data

• Hazardous Substances Data: 178979-44-7(Hazardous Substances Data)

Usage

General Description

{5-[(3-chlorophenyl)sulfanyl]-4-(1-methylethyl)-1-propyl-1H-imidazol-2-yl}methyl carbamate is a chemical compound with potential applications in pharmaceuticals and agriculture. It is a carbamate derivative consisting of an imidazole ring with a methyl carbamate group attached to it. The compound also contains a thiol group and a 3-chlorophenyl group, which may contribute to its chemical properties and potential uses. As a carbamate, it may have insecticidal or acaricidal properties, and its imidazole ring could also suggest potential biological activity as an antifungal or antimicrobial agent. Additionally, the presence of the 3-chlorophenyl group may indicate potential for use in medicinal chemistry as a scaffold for drug development. Further research and testing would be necessary to fully elucidate the properties and potential uses of this compound.

Relevant articles and documents

Imidazole derivatives as anti-HIV agents

An imidazole derivative represented by general formula (I) or a salt thereof, having the effect of specifically inhibiting the growth of HIV as a pathogenic virus and being reduced in toxicity. In said formula R1 represents hydrogen, C1 -C20 alkyl, C2 -C7 alkenyl, C4 -C12 cycloalkylalkyl, etc.; R2 represents C1 -C6 alkyl, C1 -C6 acyl, hydroxyiminomethyl, hydrazonomethyl or --(CH2)n--R4 (R4 being halogeno, alkoxy, hydroxy, etc.; and n being an integer of 1 to 3); R3 represents substituted or unsubstituted C1 -C6 alkyl; X and Y represent each independently hydrogen, C1 -C3 alkyl, halogeno, or nitro; and Z represents S, SO, SO2 or CH2. STR1