299215-38-6

Basic information

• Product Name: 2-(2-BROMOPHENYL)-2-(DIMETHYLAMINO)ACETONITRILE
• CAS NO: 299215-38-6
• Molecular Formula: C₁₀H₁₁BrN₂
• Molecular Weight: 239.11
• Mol File: 299215-38-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(2-BROMOPHENYL)-2-(DIMETHYLAMINO)ACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-BROMOPHENYL)-2-(DIMETHYLAMINO)ACETONITRILE(299215-38-6)
• EPA Substance Registry System: 2-(2-BROMOPHENYL)-2-(DIMETHYLAMINO)ACETONITRILE(299215-38-6)

Safety Data

• Hazardous Substances Data: 299215-38-6(Hazardous Substances Data)

Usage

General Description

2-(2-Bromophenyl)-2-(dimethylamino)acetonitrile is a chemical compound with the molecular formula C11H11BrN2. It is a nitrile compound that contains a bromine-substituted benzene ring and a dimethylamino group attached to a acetonitrile functional group. 2-(2-BROMOPHENYL)-2-(DIMETHYLAMINO)ACETONITRILE is used in organic synthesis and as a reagent in chemical reactions. It is known for its potential as a versatile building block in the preparation of various pharmaceutical and agrochemical agents. Additionally, it has been studied for its potential biological activities, such as antiproliferative and anticancer properties.

Upstream product

• 143-33-9 sodium cyanide 
• 506-59-2 N,N-dimethylammonium chloride 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 299215-79-5 (E)-1-(2-bromophenyl)-N,N-dimethyl-2-(4,5-dimethoxy-2-iodophenyl)ethenylamine 
• 299216-08-3 4-(5-bromo-1,3-benzodioxol-6-yl)-5-(2-bromophenyl)isoxazole 
• 299215-94-4 1-(2-bromophenyl)-2-(4,5-dimethoxy-2-iodophenyl)ethanone 
• 299215-92-2 2-(2-bromo-4,5-dimethoxyphenyl)-1-(2-bromophenyl)ethanone 
• 299215-96-6 2-(2-bromo-4,5-methylenedioxyphenyl)-1-(2-bromophenyl)ethanone 
• 299215-98-8 4,5-bis(2-bromophenyl)isoxazole 
• 299215-84-2 1,2-bis(2-bromophenyl)ethanone 
• 299215-65-9 (E)-1,2-bis(2-bromophenyl)-N,N-dimethylethenylamine 
• 54616-47-6 o-bromo-N,N'-dimethylbenzamide 
• 299215-76-2 (E)-2-(2-bromo-4,5-dimethoxyphenyl)-1-(2-bromophenyl)-N,N-dimethylethenylamine 
• 299215-82-0 (E)-2-(2-bromo-4,5-methylenedioxyphenyl)-1-(2-bromophenyl)-N,N-dimethylethenylamine 

Relevant articles and documents

A Convenient Strategy for the Synthesis of 4,5-Bis(o-haloaryl)isoxazoles

A series of new 1,2-bis(o-haloaryl)ethanones is efficiently prepared and applied to the synthesis of 4,5-bis(o-haloaryl)isoxazoles. Isolation of intermediate hydroxyisoxazolines, which are structurally examined, provides a definitive proof for a heterocyclization mechanism based on an amine exchange process. The isolation and X-ray crystallographic studies of significant side products such as benzamides and triarylpropionitriles are also described.