1380397-32-9

Basic information

• Product Name: 2,4,6-tribromo-1-(iodomethyl)benzene
• Synonyms: 2,4,6-tribromo-1-(iodomethyl)benzene
• CAS NO: 1380397-32-9
• Molecular Weight: 454.725
• Mol File: 1380397-32-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,4,6-tribromo-1-(iodomethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tribromo-1-(iodomethyl)benzene(1380397-32-9)
• EPA Substance Registry System: 2,4,6-tribromo-1-(iodomethyl)benzene(1380397-32-9)

Safety Data

• Hazardous Substances Data: 1380397-32-9(Hazardous Substances Data)

Upstream product

• 54459-64-2 2,4,6-tribromo-1-(bromomethyl)benzene 

Downstream Products

• 1380397-34-1 2,2-dimethyl-3-(2-phenylbenzoyl)-4-(2,4,6-tribromobenzyl)-oxazolidin-5-one 
• 1380397-38-5 2-(2-phenylbenzamido)-3-(2,4,6-tribromophenyl)propanoic acid 
• 1380397-36-3 methyl 2-(2-phenylbenzamido)-3-(2,4,6-tribromophenyl)propanoate 
• 1380397-37-4 methyl 2-amino-3-(2,4,6-tribromophenyl)propanoate 

Relevant articles and documents

Absolute asymmetric synthesis of tertiary α-amino acids

Frozen: The spontaneous crystallization of an achiral compound in a chiral conformation is used as the unique source of chirality in an absolute asymmetric synthesis of tertiary amino acids. The dynamic axial chirality of tertiary aromatic amides is frozen in a crystal (see picture) and is responsible for the stereoselectivity of the deprotonation/alkylation (see scheme). α-Amino acid derivatives are synthesized in up to 96% ee. Copyright