30738-49-9

Basic information

• Product Name: DIBROMOBENZILIC ACID
• Synonyms: bis(4-bromophenyl)glycolic acid;4,4'-Dibromobenzilic acid;4-Bromo-α-(4-bromophenyl)-α-hydroxybenzeneacetic acid;Bis(4-bromophenyl)hydroxyacetic acid
• CAS NO: 30738-49-9
• Molecular Formula: C₁₄H₁₀Br₂O₃
• Molecular Weight: 386.0354
• EINECS: 250-318-0
• Mol File: 30738-49-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 517.9°Cat760mmHg
• Flash Point: 267°C
• Appearance: /
• Density: 1.832g/cm³
• Vapor Pressure: 1.5E-11mmHg at 25°C
• Refractive Index: 1.665
• CAS DataBase Reference: DIBROMOBENZILIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: DIBROMOBENZILIC ACID(30738-49-9)
• EPA Substance Registry System: DIBROMOBENZILIC ACID(30738-49-9)

Safety Data

• Hazardous Substances Data: 30738-49-9(Hazardous Substances Data)

Usage

General Description

Dibromobenzilic acid, also known as 2,3-dibromo-3-phenylpropanoic acid, is a chemical compound with the molecular formula C9H8Br2O2. It is a white crystalline solid that is soluble in organic solvents such as ether and chloroform. Dibromobenzilic acid is used in organic synthesis as a reagent for the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It is also used as a research tool in studies of chemical reactions and mechanisms. Dibromobenzilic acid is a versatile compound that has applications in a wide range of fields within the chemical industry.

InChI:InChI=1/C14H10Br2O3/c15-11-5-1-9(2-6-11)14(19,13(17)18)10-3-7-12(16)8-4-10/h1-8,19H,(H,17,18)

Upstream product

• 35578-47-3 4,4'-dibromobenzil 
• 141-52-6 sodium ethanolate 
• 4254-18-6 1,2-bis(4-bromophenyl)-2-hydroxyethan-1-one 
• 1122-91-4 4-bromo-benzaldehyde 
• 18181-80-1 bromopropylate 
• 108-86-1 bromobenzene 
• 298-12-4 Glyoxilic acid 

Downstream Products

• 3988-03-2 bis(4-bromophenyl)methanone 
• 58132-31-3 5,5-bis(4-bromophenyl)imidazolidine-2,4-dione 
• 134871-23-1 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-pyrrolidin-1-yl-propyl ester 
• 134871-25-3 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-piperidin-1-yl-propyl ester 
• 134871-28-6 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-azepan-1-yl-ethyl ester 
• 134871-26-4 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-morpholin-4-yl-ethyl ester 
• 134871-29-7 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-azepan-1-yl-propyl ester 
• 134871-27-5 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-morpholin-4-yl-propyl ester 
• 134871-24-2 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-piperidin-1-yl-ethyl ester 
• 134871-19-5 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-dimethylamino-ethyl ester 
• 134871-20-8 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-dimethylamino-propyl ester 
• 134871-21-9 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-diethylamino-ethyl ester 
• 134871-22-0 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-diethylamino-propyl ester 
• 23197-74-2 4,4'-Dibrombenzilsaeure-methylester 

Relevant articles and documents

Synthesis method and application of 2, 2, 2 (4-bromophenyl)-2-hydroxyacetic acid

The invention provides a synthesis method and application of 2, 2-2 (4-bromophenyl)-2-hydroxyacetic acid, and the synthesis method is characterized in that under the catalysis of an alkaline condition, 2, 2-2 (4-bromophenyl)-2-hydroxyacetic acid bromobenzene and glyoxylic acid are subjected to addition, oxidation, secondary addition and acidification to prepare a bromopropylate key intermediate 2, 2-2 (4-bromophenyl)-2-hydroxyacetic acid. The 2, 2-2 (4-bromophenyl)-2-glycolic acid prepared by the preparation method disclosed by the invention is relatively high in yield, the utilization rate of glyoxylic acid is relatively high, and the 2, 2-2 (4-bromophenyl)-2-glycolic acid prepared by the preparation method disclosed by the invention is used for preparing bromopropylate.

Development of an enzyme-linked immunosorbent assay for determination of the miticide bromopropylate

This paper reports for the first time the development of an immunoassay for the analysis of the miticide bromopropylate (BP). The chemical structure of the immunizing haptens was designed to maximize the recognition of the bis-bromophenyl group of BP. Thu

4,4'-DIBROMOBENZYLIC ACID &β- AND &γ-AMINOALKYL ESTER HYDROCHLORIDES AND THEIR BIOLOGICAL PROPERTIES

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