55048-80-1

Basic information

• Product Name: P-BROMOPHENYLARSONIC ACID
• Synonyms: P-BROMOPHENYLARSONIC ACID;4-(Bromophenyl)-arsonic acid
• CAS NO: 55048-80-1
• Molecular Formula: C₆H₆AsBrO₃
• Molecular Weight: 280.94
• Mol File: 55048-80-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 473.4°C at 760 mmHg
• Flash Point: 240.1°C
• Appearance: /
• Vapor Pressure: 9.08E-10mmHg at 25°C
• PKA: pK1: 3.25;pK2: 8.19 (25°C)
• CAS DataBase Reference: P-BROMOPHENYLARSONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: P-BROMOPHENYLARSONIC ACID(55048-80-1)
• EPA Substance Registry System: P-BROMOPHENYLARSONIC ACID(55048-80-1)

Safety Data

• Hazardous Substances Data: 55048-80-1(Hazardous Substances Data)

Usage

General Description

P-Bromophenylarsonic acid is a chemical compound that belongs to the family of organoarsenic compounds. It is a derivative of arylarsonic acid, commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The compound is a white to off-white powder that is sparingly soluble in water and organic solvents. P-Bromophenylarsonic acid is primarily used as a raw material in the production of veterinary drugs and antibacterial agents for animal feed. It is also used in the manufacturing of dyes and pigments. However, it is important to handle and dispose of this compound with care, as it is toxic and can have harmful effects on human health and the environment.

InChI:InChI=1/C6H6AsBrO3/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H,(H2,9,10,11)

Upstream product

• 17333-82-3 4-bromo-benzenediazonium ion 
• 73013-32-8 p-bromophenylarsine dichloride 
• 2028-85-5 (4-bromophenyl)diazonium chloride 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 73013-32-8 p-bromophenylarsine dichloride 
• 88861-63-6 p-Bromophenyldibromoarsine 
• 860602-62-6 (4-bromo-3-nitro-phenyl)-arsonic acid 
• 141033-46-7 bis(2,3,7,8,b,h)-(1NN-dimethylamidobenzo)-5-arsa-5-parabromophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane 
• 141033-41-2 bis(2,3,7,8,b,h)-(1NN-diethylamidobenzo)-5-arsa-5-parabromophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane 
• 6306-93-0 tris(4-bromophenyl)arsine 
• 4964-26-5 tris-(4-bromo-phenyl)-arsine oxide 
• 6306-92-9 tris-(4-bromo-3-nitro-phenyl)-arsine 
• 861788-42-3 (4-bromo-phenyl)-iodo-methyl-arsine 
• 861788-40-1 (4-bromo-phenyl)-methyl-phenyl-arsine 
• 873413-35-5 tris-(4-bromo-3-nitro-phenyl)-arsine oxide 
• 121-19-7 roxarsone 
• 91858-71-8 [Mn(p-BrC₆H₄AsO₃)(OH)(H₂O)3]2 

Relevant articles and documents

Arylarsonate- And Phosphonate-Capped Polyoxomolybdates, [(RC6H4As)2Mo6O24]n-and [(R′C6H4P)2Mo5O21]n-

We report on the synthesis and structural characterization of four arylarsonate- and phosphonate-capped polyoxomolybdates that exhibit different organic substituents in the para position of the phenyl group. The reaction of arylarsonates (RAsO3, wherein R

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.