60593-34-2

Usage

Uses

Used in Pharmaceutical Synthesis:
(2-bromophenyl)arsonic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs with potential therapeutic benefits.
Used in Agriculture as Insecticide and Herbicide:
Due to its insecticidal and herbicidal properties, (2-bromophenyl)arsonic acid is employed as an active ingredient in agricultural chemicals. It helps control pests and weeds, thereby protecting crops and increasing agricultural productivity.
Used in Animal Feed as a Growth Promoter:
(2-bromophenyl)arsonic acid has been used as a growth promoter in animal feed. Its inclusion in feed formulations can enhance the growth rate and overall health of livestock, contributing to the efficiency of meat and dairy production.
Used in Veterinary Medicine for Treating Infections:
In the field of veterinary medicine, (2-bromophenyl)arsonic acid serves as a medicine for treating infections in animals. Its antimicrobial properties make it effective against a range of pathogens, ensuring the health and well-being of animals under veterinary care.

Upstream product

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

Downstream Products

• 856089-87-7 [2-(5-nitro-[8]quinolylamino)-phenyl]-arsonic acid 
• 1758-48-1 o-phenylene-bis-arsonic acid 
• 860602-64-8 (2-bromo-5-nitro-phenyl)-arsonic acid 
• 860236-50-6 [2-(2,4-dimethyl-anilino)-phenyl]-arsonic acid 
• 860239-66-3 [2-(3,4-dichloro-anilino)-phenyl]-arsonic acid 
• 57170-65-7 o-Bromphenylarsindichlorid 
• 88861-64-7 o-Bromophenyldibromoarsine 
• 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 
• 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 

Relevant academic research and scientific papers

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.

Carbonylvanadium, -manganese and -molybdenum Complexes of the Ligands o-C6H4EPh2(E'Ph2) (E, E' = P, As, Sb, Bi) and cis-Ph2PCH=CHPPh2

The photo-induced reaction between the complexes (1), η5-C5H5V(CO)4 (2), η5-C5H5Mn(CO)3 (3) or η5-C5H5Mo(CO)3CH3 (4) and the ligands o-C6H4EPh2(E'Ph2) (E = E' = P: a; E = P, E' = As: b; E = E' = As: c; E = P, E' = Sb: d; E = P, E' = Bi: e; E = As, E' = Sb: f) and cis-Ph2PCH=CHPPh2 (g), L, yields - depending on the steric requirement of L - the compounds L ( = cis-V(CO)4(-), cis-CpV(CO)2, CpMn(CO), CpMo(CO)CH3; L = a, b, c, g), L ( = V(CO)5(-), L = d; = CpV(CO)3, L = d, e; = CpMn(CO)2, L = e) or mixtures of L and L (, = V(CO)4,5, L = e, f; , = CpV(CO)2,3, L = f).In the mono-substituted species L coordination (as indicated by the 51V NMR spectra) occurs through EPh2 and E'Ph2, which is explained by a reaction path via a lable chelate 5-ring structure.Shielding of the 51V nucleus decreases in the order g > SbPh2 > PPh2 > AsPh2 > BiPh2 (derivatives of 1) and g > SbPh2 > PPh2 > BiPh2 > AsPh2 (derivatives of 2), and is smaller in the rigid chelates incorporating the o-phenylene ligands than in the more flexible structures of phospha- and arsabutane complexes.This fact is discussed in terms of hindered ?-overlap due to distortion of the EVE angle, which also results in an increase of CO valence force constants in rigid chelates. 31P coordination shifts increase according to dppe a g and arphos b (dppe = Ph2P(CH2)2PPh2, arphos = Ph2As(CH2)2PPh2). 31P NMR spectra of the molybdenum complexes suggest that the basic geometry for 4a and 4b likely is tetragonal pyramidal, while the preferred structure for 4g appears to be the trigonal bipyramid with the ligand in equatorial positions.The crystal and molecular structure of 1a is reported.The complex crystallizes in the space group C2/c (a = 2196.0, b = 1080.1, c = 2022.7 pm, β = 124.6 deg).The most striking result is the small PVP angle of 80.8 (0.2) deg.Optimized methods for the synthesis of the ligands a-f are described; the ligands are characterized by their mass spectra. - Keywords: Carbonylphosphinevanadium, Vanadium-NMR; Phosphorus-NMR