634-89-9

Basic information

• Product Name: Benzene,1,2,3,5-tetrabromo-
• Synonyms: 1,2,3,5-Tetrabromobenzene
• CAS NO: 634-89-9
• Molecular Formula: C6H2 Br4
• Molecular Weight: 393.698
• Mol File: 634-89-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene,1,2,3,5-tetrabromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene,1,2,3,5-tetrabromo-(634-89-9)
• EPA Substance Registry System: Benzene,1,2,3,5-tetrabromo-(634-89-9)

Safety Data

• Hazardous Substances Data: 634-89-9(Hazardous Substances Data)

Upstream product

• 106-40-1 4-bromo-aniline 
• 147-82-0 2,4,6-tribromoaniline 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 626-39-1 1,3,5-trisbromobenzene 
• 591-19-5 m-Bromoaniline 
• 108-95-2 phenol 
• 305-80-6 4-diazobenzenesulfonic acid 
• 608-90-2 pentabromobenzene 
• 363598-44-1 (2,4,6-tribromophenyl)trimethylsilane 
• 686349-64-4 2,3,4,6-tetrabromo-benzenesulfonic acid 
• 10035-10-6 hydrogen bromide 
• 103-84-4 Acetanilid 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 626-39-1 1,3,5-trisbromobenzene 
• 22230-07-5 1,2,3,5-tetrabromo-4,6-dinitro-benzene 
• 686349-64-4 2,3,4,6-tetrabromo-benzenesulfonic acid 
• 607-99-8 2,4,6-tribromoanisole 
• 73557-60-5 3,4,5-tribromo-anisole 
• 73931-44-9 2,3,5-tribromoanisole 
• 59080-33-0 2,4,6-tribromobiphenyl 
• 115245-08-4 3,4,5-tribromo-biphenyl 
• 108-86-1 bromobenzene 
• 71-43-2 benzene 
• 633-12-5 2,4,6-tribromobenzoic acid 
• 87976-24-7 2,3,4,6-tetrabromobenzoic acid 
• 87976-25-8 2,3,5,6-tetrabromobenzoic acid 
• 103068-20-8 1-bromo-3,5-diphenylbenzene 

Relevant articles and documents

Regioselectivity of reductive debromination of substituted pentabromobenzenes with sodium tert-butoxide in DMSO

The regioselectivity of reductive debromination of substituted pentabromobenzenes C6Br5X (X = NH2, OMe, Me, H, Cl, F, and NO2) under the action of ButONa in DMSO containing ButOH has been studied. The reaction followed the halophilic mechanism via carbanions.

Aprotic diazotization in the presence of cuprous cyanide

In a procedure of extreme simplicity and rapidity a mixture of an aromatic primary amine, copper (I) cyanide and an alkyl nitrite in dimethyl sulphoxide yielded fair to moderate yields of the corresponding nitriles. Side processes observed were reduction (NH2&[H), nitration (NH2←NO2) and hydroxylation (NH2&[OH). In the case of polyhaloanilines halogen dance products could be detected.