DIBROMOBENZILIC ACID

Base Information

  • Chemical Name: DIBROMOBENZILIC ACID
  • CAS No.: 30738-49-9

Factory supply DIBROMOBENZILIC ACID 30738-49-9 with sufficient stock and high standard

  • Molecular Formula: C14H10 Br2 O3
  • Molecular Weight: 386.04
  • Vapor Pressure: 1.5E-11mmHg at 25°C 
  • Boiling Point: 517.9°Cat760mmHg 
  • Flash Point: 267°C 
  • PSA： 57.53000 
  • Density: 1.832g/cm3 
  • LogP: 3.53210 

DIBROMOBENZILIC ACID(Cas 30738-49-9) 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)

30738-49-9 Relevant articles

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

-

, (2022/01/04)

The invention provides a synthesis metho...

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

Singh, Neetu,Singh, Satish Kumar,Khanna,Singh, Krishna Nand

experimental part, p. 2419 - 2422 (2011/05/09)

Ionic liquid in conjugation with KOH bri...

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

Ramon-Azcon, Javier,Sanchez-Baeza, Francisco,Sanvicens, Nuria,Marco, M.-Pilar

experimental part, p. 375 - 384 (2010/05/19)

This paper reports for the first time th...

Microwave-assisted heterogeneous benzil-benzilic acid rearrangement

Yu, Hui-Ming,Chen, Same-Ting,Tseng, Min-Jen,Chen, Shui-Tein,Wang, Kung-Tsung

, p. 62 - 63 (2007/10/03)

A new procedure for carrying out the ben...

30738-49-9 Process route

4-bromo-benzaldehyde
1122-91-4

4-bromo-benzaldehyde

2,2-bis(4-bromophenyl)-2-hydroxyacetic acid
30738-49-9

2,2-bis(4-bromophenyl)-2-hydroxyacetic acid

Conditions
Conditions Yield
4-bromo-benzaldehyde; With oxygen; 1-butyl-3-methylimidazolium Tetrafluoroborate; potassium hydroxide; at 60 ℃; for 0.333333h; Neat (no solvent); Microwave irradiation;
With hydrogenchloride; In water; at 20 ℃;
78%
Multi-step reaction with 3 steps
1: 91.8 percent / NaCN / ethanol; H2 O / 0.33 h / Heating
2: 87 percent / copper sulfate, pyridine, O2 / H2 O / 2 h / Heating
3: 93 percent / aq. KOH / ethanol / 1 h / Heating
With pyridine; potassium hydroxide; copper(I) sulfate; sodium cyanide; oxygen; In ethanol; water;
C<sub>14</sub>H<sub>9</sub>Br<sub>2</sub>O<sub>3</sub><sup>(1-)</sup>*Na<sup>(1+)</sup>

C14 H9 Br2 O3 (1-) *Na(1+)

2,2-bis(4-bromophenyl)-2-hydroxyacetic acid
30738-49-9

2,2-bis(4-bromophenyl)-2-hydroxyacetic acid

Conditions
Conditions Yield
With hydrogenchloride; In water; toluene; at 10 - 20 ℃; pH=2 - 3;
78%

30738-49-9 Upstream products

  • 35578-47-3
    35578-47-3

    4,4'-dibromobenzil

  • 141-52-6
    141-52-6

    sodium ethanolate

  • 4254-18-6
    4254-18-6

    1,2-bis(4-bromophenyl)-2-hydroxyethan-1-one

  • 1122-91-4
    1122-91-4

    4-bromo-benzaldehyde

30738-49-9 Downstream products

  • 3988-03-2
    3988-03-2

    bis(4-bromophenyl)methanone

  • 58132-31-3
    58132-31-3

    5,5-bis(4-bromophenyl)imidazolidine-2,4-dione

  • 134871-25-3
    134871-25-3

    Bis-(4-bromo-phenyl)-hydroxy-acetic acid 3-piperidin-1-yl-propyl ester

  • 134871-26-4
    134871-26-4

    Bis-(4-bromo-phenyl)-hydroxy-acetic acid 2-morpholin-4-yl-ethyl ester

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