178979-68-5

Basic information

• Product Name: 1-{5-[(3,5-dichlorophenyl)sulfanyl]-1-(fluoromethyl)-4-(1-methylethyl)-1H-imidazol-2-yl}methanamine
• CAS NO: 178979-68-5
• Molecular Formula: C₁₄H₁₆Cl₂FN₃S
• Molecular Weight: 348.2663
• Mol File: 178979-68-5.mol

Chemical Properties

• Boiling Point: 480.4°C at 760 mmHg
• Flash Point: 244.3°C
• Density: 1.4g/cm³
• Vapor Pressure: 2.17E-09mmHg at 25°C
• Refractive Index: 1.623
• CAS DataBase Reference: 1-{5-[(3,5-dichlorophenyl)sulfanyl]-1-(fluoromethyl)-4-(1-methylethyl)-1H-imidazol-2-yl}methanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{5-[(3,5-dichlorophenyl)sulfanyl]-1-(fluoromethyl)-4-(1-methylethyl)-1H-imidazol-2-yl}methanamine(178979-68-5)
• EPA Substance Registry System: 1-{5-[(3,5-dichlorophenyl)sulfanyl]-1-(fluoromethyl)-4-(1-methylethyl)-1H-imidazol-2-yl}methanamine(178979-68-5)

Safety Data

• Hazardous Substances Data: 178979-68-5(Hazardous Substances Data)

Usage

Chemical structure

A complex organic compound with multiple functional groups and a heterocyclic ring system.

Fluoromethyl group

A functional group containing a carbon atom bonded to a fluorine atom, which can influence the compound's reactivity and properties.

Sulfanyl group

A sulfur atom bonded to another atom or group, which can contribute to the compound's reactivity and potential biological activity.

Imidazol-2-yl group

A heterocyclic ring system with a nitrogen atom at the 2-position, which can be involved in various biological interactions and may contribute to the compound's pharmacological properties.

1-methylethyl (isopropyl) group

A branched alkyl group with three carbon atoms, which can affect the compound's steric properties and lipophilicity.

Potential pharmaceutical properties

The compound's complex structure and functional groups suggest it may have specific and potent effects on biological processes, making it a candidate for drug development and medical research.

Interaction with biological systems

Due to its diverse functional groups and complex structure, the compound may have the ability to interact with various biological targets, such as enzymes, receptors, or other proteins.

Applications in drug development

The compound's potential to modulate biological processes could make it a valuable tool for the development of new therapeutic agents.

Contributions to biochemistry and pharmacology

The study of this compound's interactions with biological systems can help further our understanding of biochemistry and pharmacology, potentially leading to the discovery of new mechanisms of action or novel drug targets.

Upstream product

• 178981-75-4 2-azidomethyl-5-(3,5-dichlorophenylthio)-1-fluoromethyl-4-isopropyl-1H-imidazole 

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