855836-62-3

Basic information

• Product Name: 2-BROMO-3-CHLOROPHENOL
• Synonyms: 2-BROMO-3-CHLOROPHENOL;Phenol, 2-broMo-3-chloro-
• CAS NO: 855836-62-3
• Molecular Formula: C₆H₄BrClO
• Molecular Weight: 207.45
• Product Categories: pharmacetical
• Mol File: 855836-62-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 55.5 °C
• Boiling Point: 233.0±20.0 °C(Predicted)
• Appearance: /
• Density: 1.788±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 7.47±0.10(Predicted)
• CAS DataBase Reference: 2-BROMO-3-CHLOROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-3-CHLOROPHENOL(855836-62-3)
• EPA Substance Registry System: 2-BROMO-3-CHLOROPHENOL(855836-62-3)

Safety Data

• Hazardous Substances Data: 855836-62-3(Hazardous Substances Data)

Usage

General Description

2-Bromo-3-Chlorophenol is a chemical compound with the formula C6H4BrClO. It is a derivative of phenol, containing both bromine and chlorine substituents. 2-Bromo-3-Chlorophenol is commonly used in the production of pharmaceuticals, dyes, and insecticides. It is also utilized as a disinfectant and antiseptic due to its antimicrobial properties. 2-BROMO-3-CHLOROPHENOL is a white crystalline solid with a distinctive odor, and it is soluble in organic solvents such as ethanol and acetone. It is important to handle this compound with care, as it is toxic and can cause skin and eye irritation upon contact. Additionally, it is harmful if ingested or inhaled, and may cause environmental damage if not properly handled and disposed of.

Upstream product

• 108-43-0 3-monochlorophenol 
• 159390-33-7 3-chlorophenyl N,N-diethylcarbamate 
• 863870-78-4 O-2-bromo-3-chlorophenyl N,N-diethylcarbamate 

Downstream Products

• 872274-09-4 3-bromo-4-chloro-2-hydroxybenzaldehyde 
• 96558-73-5 2-bromo-3-chloro-aniline 
• 1287791-76-7 N-(2-bromo-3-chlorophenyl)-2-hydroxy-2-methylpropanamide 
• 1287791-67-6 2-(2-bromo-3-chlorophenoxy)-2-methylpropanamide 
• 174913-08-7 2-bromo-3-chloro-anisole 

Relevant articles and documents

Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles

2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner.

A new and efficient synthesis of 4-functionalized benzo[6]furans from 2,3-dihalophenols

Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other proc