132331-08-9

Basic information

• Product Name: Phenol, 3-amino-2,4,6-tribromo-
• CAS NO: 132331-08-9
• Molecular Formula: C6H4Br3NO
• Molecular Weight: 345.816
• Mol File: 132331-08-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 117-118 °C
• Boiling Point: 284.5±35.0 °C(Predicted)
• Density: 2.493±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Phenol, 3-amino-2,4,6-tribromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-amino-2,4,6-tribromo-(132331-08-9)
• EPA Substance Registry System: Phenol, 3-amino-2,4,6-tribromo-(132331-08-9)

Safety Data

• Hazardous Substances Data: 132331-08-9(Hazardous Substances Data)

Upstream product

• 618-49-5 3-hydroxybenzamide 
• 591-27-5 m-Hydroxyaniline 
• 99-09-2 3-nitro-aniline 
• 108-46-3 recorcinol 
• 554-84-7 meta-nitrophenol 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 
• 64297-64-9 2-iodoxybenzoic acid 
• 65-49-6 4-Aminosalicylic acid 
• 69076-62-6 2,4,6-tribromo-3-nitrophenol 

Downstream Products

• 63561-48-8 2-acetoxy-1,3,5-tribromo-4-diacetylamino-benzene 

Relevant articles and documents

Determination of isoniazid in drugs with 2-iodoxybenzoate

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Regioselective, photochemical bromination of aromatic compounds using N-bromosuccinimide

Regioselective nuclear bromination of aromatic compounds is investigated with N-bromosuccinimide as the brominating agent under UV irradiation to afford the corresponding brominated compounds. The reaction proceeds at ambient temperature (30 ± 2 °C) without any catalyst. In most of the reactions, regioselectively mono-brominated products are obtained in good to high yields. The conversion and selectivity for bromination depend on the nature of the substituent on the aromatic ring.

Solid-state Nuclear Bromination of Some Phenols by N-Bromosuccinimide

Treatment of crystalline dimethylphenols and hydroquinones with N-bromosuccinimide leads rapidly and regioselectively to ring-substituted products.