948549-53-9

Basic information

• Product Name: 3-BROMO-4-CHLOROBENZONITRILE
• Synonyms: 3-BROMO-4-CHLOROBENZONITRILE;3-broMo -4-benzene nitrile
• CAS NO: 948549-53-9
• Molecular Formula: C₇H₃BrClN
• Molecular Weight: 216.46242
• Mol File: 948549-53-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 260.172 °C at 760 mmHg
• Flash Point: 111.148 °C
• Appearance: /
• Density: 1.74 g/cm³
• Vapor Pressure: 0.0124mmHg at 25°C
• Refractive Index: 1.623
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 3-BROMO-4-CHLOROBENZONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-4-CHLOROBENZONITRILE(948549-53-9)
• EPA Substance Registry System: 3-BROMO-4-CHLOROBENZONITRILE(948549-53-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• HazardClass: IRRITANT
• Hazardous Substances Data: 948549-53-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H3BrClN/c8-6-3-5(4-10)1-2-7(6)9/h1-3H

Upstream product

• 623-03-0 4-Cyanochlorobenzene 

Downstream Products

• 863868-30-8 4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile 
• 1613393-74-0 4-chloro-3-[(3aR,5S,7aS)-5-methyltetrahydro-1H-pyrano[3,4-c][1,2]oxazol-7a(7H)-yl]benzonitrile 

Relevant articles and documents

A selenazole armor acid compounds and salts thereof

The invention relates to a selenazole acid compound as shown in the formula I or a pharmaceutically acceptable salt, aquo-complex and solvate, and provides a preparation method of the compound and an application of the compound in preparation of a medicin

Chemoselective bromodeboronation of organotrifluoroborates using tetrabutylammonium tribromide: Application in (Z)-dibromoalkene syntheses

(Chemical Equation Presented) Tetrabutylammonlum trlbromlde (TBATB) has been found to be a unique bromodeboronatlon reagent for organotrlf luoroborates. When compared to previously reported bromodeboronatlon methods, the mild and metal-free reaction conditions tolerate a wider range of functional groups. High reglo- and chemoselectlvlty are observed In the presence of both unsaturated carbon-carbon bonds and aldehyde functional groups. An efficient synthetic route to (Z)-dlbromoalkenes from terminal alkynes has been developed using the TBATB-medlated bromodeboronatlon as a key step.