173026-22-7

Basic information

• Product Name: 2-bromo-α,α-dimethylbenzeneacetamide
• Synonyms: 2-bromo-α,α-dimethylbenzeneacetamide
• CAS NO: 173026-22-7
• Molecular Weight: 242.115
• Mol File: 173026-22-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-bromo-α,α-dimethylbenzeneacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-α,α-dimethylbenzeneacetamide(173026-22-7)
• EPA Substance Registry System: 2-bromo-α,α-dimethylbenzeneacetamide(173026-22-7)

Safety Data

• Hazardous Substances Data: 173026-22-7(Hazardous Substances Data)

Upstream product

• 1422148-87-5 N-acetyl-2-(2-bromophenyl)-2-methylpropanamide 
• 57775-06-1 2-(2-bromophenyl)-2-methylpropanenitrile 

Downstream Products

• 19155-24-9 3,3-dimethyloxindole 
• 114081-14-0 1-benzyl-3,3-dimethyl-1,3-dihydro-indol-2-one 
• 36797-34-9 3,3-dimethyl-1-tosylindolin-2-one 
• 1422148-84-2 N-benzyl-2-(2-bromophenyl)-2-methylpropanamide 
• 1422148-87-5 N-acetyl-2-(2-bromophenyl)-2-methylpropanamide 
• 1422148-86-4 2-(2-bromophenyl)-2-methyl-N-tosylpropanamide 
• 1422148-83-1 2-(2-bromophenyl)-N,2-dimethylpropanamide 
• 1566544-00-0 2-methyl-2-(2-((triethylsilyl)ethynyl)phenyl)propanamide 
• 1566543-20-1 2-(2-(2-(5-chloro-2-((1-methyl-1H-pyrazol-4-yl)amino)pyrimidin-4-yl)ethyl)phenyl)2-methylpropanamide 
• 1566544-03-3 2-(2-(2-(2,5-dichloropyrimidin-4-yl)ethyl)phenyl)-2-methylpropanamide 
• 1566544-02-2 2-(2-((2,5-dichloropyrimidin-4-yl)ethynyl)phenyl)-2-methylpropanamide 
• 1566544-01-1 2-(2-ethynylphenyl)-2-methylpropanamide 
• 173026-23-8 2-bromo-α,α-dimethylbenzenemethanamine 

Relevant articles and documents

VEGFR3 INHIBITORS

This invention relates to a compound of the formula (I): The invention also relates to processes for the preparation of the compound of the formula (I), pharmaceutical agents or compositions containing the compound or a method of using the compound for th

Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.

Compounds having a benzisoselen-azoline and -azine structure, method for preparing same and therapeutic uses thereof

The invention concerns novel benzisoselen-azoline and -azine derivatives. These novel derivatives have the following general formula (II): STR1 where: R1 to R8 and R10 have various meanings, in particular H, alkyl, etc . .