760212-40-6

Basic information

• Product Name: 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole
• Synonyms: 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole;2-(3-broMophenyl)-1-phenyl-1H-benzo[d]iMidazole;2-(3-BroMophenyl)-1-phenylbenziMidazole, 98%;1H-Benzimidazole,2-(3 -bromophenyl)-1-phenyl;2-(3,5-dibromophenyl)-1-phenyl-1H-benzimidazole;1H-Benzimidazole,2-(2-bromophenyl)-1-phenyl-;2-(3-broMophenyl)-1-phenyl-1H-1,3-benzodiazole
• CAS NO: 760212-40-6
• Molecular Formula: C₁₉H₁₃BrN₂
• Molecular Weight: 349.24
• Mol File: 760212-40-6.mol
• Article Data: 12

Chemical Properties

• Melting Point: 123.0 to 127.0 °C
• Boiling Point: 513.6 °C at 760 mmHg
• Flash Point: 264.4 °C
• Appearance: /
• Density: 1.38 g/cm³
• Vapor Pressure: 1.17E-10mmHg at 25°C
• Refractive Index: 1.671
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole(760212-40-6)
• EPA Substance Registry System: 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole(760212-40-6)

Safety Data

• Hazardous Substances Data: 760212-40-6(Hazardous Substances Data)

Usage

Description

2-(3-bromophenyl)-1-phenyl-1H-benzimidazole is a chemical compound belonging to the benzimidazole family of organic compounds. It is characterized by the presence of a bromine atom attached to the third carbon of the phenyl group, making it a brominated derivative. The benzimidazole structure of the compound provides high thermal stability and resistance to oxidation.

Uses

Used in Pharmaceutical Industry:
2-(3-bromophenyl)-1-phenyl-1H-benzimidazole is used as a pharmaceutical compound for its potential biological activities. The specific structure of the compound allows for modification to enhance its therapeutic properties and target various biological pathways.
2-(3-bromophenyl)-1-phenyl-1H-benzimidazole's high thermal stability and resistance to oxidation make it suitable for use in pharmaceutical formulations, ensuring its stability and efficacy during manufacturing and storage processes.
Furthermore, the brominated derivative nature of 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole may contribute to its unique biological activities, such as modulating specific signaling pathways or interacting with certain receptors, making it a promising candidate for the development of new drugs and therapeutic agents.

InChI:InChI=1/C19H13BrN2/c20-15-8-6-7-14(13-15)19-21-17-11-4-5-12-18(17)22(19)16-9-2-1-3-10-16/h1-13H

Upstream product

• 585-76-2 m-bromobenzoic acid 
• 3132-99-8 m-bromobenzoic aldehyde 
• 534-85-0 N-phenyl-1,2-benzenediamine 
• 1711-09-7 3-bromobenzoyl chloride 
• 952514-85-1 C₁₉H₁₅BrN₂O 

Downstream Products

• 952514-86-2 1-phenyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole 
• 1271754-06-3 C₅₇H₃₉N₅ 
• 935472-79-0 2-(3-(10-bromoanthracen-9-yl)phenyl)-1-phenyl-1H-benzo[d]imidazole 
• 1499166-97-0 9-phenyl-3,6-bis(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9H-carbazole 
• 1384321-92-9 9-(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-9H-carbazole 

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