60593-34-2

Basic information

• Product Name: (2-bromophenyl)arsonic acid
• CAS NO: 60593-34-2
• Molecular Formula: C₆H₆AsBrO₃
• Molecular Weight: 280.9356
• Mol File: 60593-34-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 489.8°C at 760 mmHg
• Flash Point: 250°C
• Vapor Pressure: 2.08E-10mmHg at 25°C
• CAS DataBase Reference: (2-bromophenyl)arsonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromophenyl)arsonic acid(60593-34-2)
• EPA Substance Registry System: (2-bromophenyl)arsonic acid(60593-34-2)

Safety Data

• Hazardous Substances Data: 60593-34-2(Hazardous Substances Data)

Usage

General Description

(2-bromophenyl)arsonic acid, also known as Diphenylhydantoin, is a chemical compound that contains an aromatic ring with a bromine atom and an arsenic atom attached to it. It is commonly used in the synthesis of pharmaceuticals and is also known for its insecticidal and herbicidal properties. The compound has also been used as a growth promoter in animal feed and as a medicine for treating infections in animals. However, it is important to note that the compound is toxic and can be harmful if not handled properly. Therefore, it should be used and handled with caution and under appropriate safety measures.

Upstream product

• 615-36-1 2-bromoaniline 
• 2045-00-3 o-arsanilic acid 
• 17333-81-2 o-bromobenzenediazonium 

Downstream Products

• 860236-50-6 [2-(2,4-dimethyl-anilino)-phenyl]-arsonic acid 
• 860239-66-3 [2-(3,4-dichloro-anilino)-phenyl]-arsonic acid 
• 861304-31-6 (2-hydroxy-5-nitro-phenyl)-arsonic acid 
• 55677-77-5 1,2-bis(diphenylarsino)benzene 
• 55677-75-3 diphenyl-(2-diphenylphosphinophenyl)-arsine 
• 57170-67-9 (2-bromophenyl)diphenylarsine 
• 57170-65-7 o-Bromphenylarsindichlorid 
• 88861-64-7 o-Bromophenyldibromoarsine 
• 860727-76-0 [2-(N-methyl-anilino)-phenyl]-arsonic acid 
• 860727-68-0 (2-o-toluidino-phenyl)-arsonic acid 
• 872275-94-0 (2-anilino-phenyl)-arsonic acid 
• 860236-55-1 (2-p-toluidino-phenyl)-arsonic acid 
• 860602-64-8 (2-bromo-5-nitro-phenyl)-arsonic acid 
• 1758-48-1 o-phenylene-bis-arsonic acid 

Relevant articles and documents

SYNTHESIS AND PROPERTIES OF ARYLARSONIC ACIDS

1.A number of arylarsonic acids with various substituents in the ortho, meta, and para positions in the benzene ring were synthesized from diazonium salts by the Bart reaction; the products were characterized by their IR spectra. 2.By the DTA method it was established that arylarsonic acid molecules were linked together through hydrogen bonds to form oligomeric associated forms. 3.The IR spectra of arylarsonic acids confirm the presence in them of strong hydrogen bonds through which they are able to undergo association into two forms differing in the symmetry of the d isposition of the As=O bonds.A form which gives a C band arises if the arsonyl oxygen participates in the formation of two hydrogen bonds simultaneously, as a result of which the molecules are linked together to form endless chains and columns.In the other form there are probably cyclic dimers with intermolecular H bonds.