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

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

Uses

Used in Organic Synthesis:
Dibromobenzilic acid is used as a reagent in organic synthesis for the production of various organic compounds. Its unique structure and properties make it a valuable component in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new and improved products in these fields.
Used in Chemical Research:
As a research tool, dibromobenzilic acid is employed in studies of chemical reactions and mechanisms. Its use in this context facilitates a deeper understanding of chemical processes, potentially leading to advancements in the chemical sciences and related industries.
Used in Pharmaceutical Industry:
Dibromobenzilic acid is used as a key intermediate in the synthesis of pharmaceuticals. Its presence in the production process aids in the creation of new medications, enhancing the range of treatments available for various health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, dibromobenzilic acid is utilized in the synthesis of agrochemicals, such as pesticides and herbicides. Its role in these processes helps to develop more effective products for agricultural use, contributing to increased crop yields and protection against pests.
Overall, dibromobenzilic acid's applications are diverse, spanning across multiple industries within the chemical sector, and its uses are continually expanding as new research and development initiatives uncover further potential applications.

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

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

Downstream Products

• 134871-29-7 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-azepan-1-yl-propyl ester 
• 1103496-15-6 methyl 4-[2,2-bis(4-bromophenyl)-2-hydroxyacetamido]butanoate 
• 21771-79-9 bis-(4-bromo-phenyl)-acetic acid 
• 23197-74-2 4,4'-Dibrombenzilsaeure-methylester 
• 134871-22-0 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-diethylamino-propyl ester 
• 134871-21-9 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-diethylamino-ethyl ester 
• 134871-20-8 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-dimethylamino-propyl ester 
• 134871-19-5 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-dimethylamino-ethyl ester 
• 134871-24-2 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-piperidin-1-yl-ethyl ester 
• 134871-27-5 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-morpholin-4-yl-propyl ester 
• 134871-26-4 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-morpholin-4-yl-ethyl ester 
• 134871-28-6 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-azepan-1-yl-ethyl ester 
• 134871-25-3 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-piperidin-1-yl-propyl ester 
• 134871-23-1 Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-pyrrolidin-1-yl-propyl ester 

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.

Ionic liquid/potassium hydroxide catalyzed solvent-free, one-pot synthesis of diarylglycolic acids from aromatic aldehydes under microwave

Ionic liquid in conjugation with KOH brings about an efficient, one-pot, green synthesis of α,α-diarylglycolic acids in reasonably high yields from aromatic aldehydes under solvent-free condition using conventional heating as well as microwave irradiation.

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

Microwave-assisted heterogeneous benzil-benzilic acid rearrangement

A new procedure for carrying out the benzil-benzilic acid rearrangement in the solid state has been developed which provides a new route to synthesize the pharmacologically interesting anticonvulsant dilantin.