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BROMOMALEIC ANHYDRIDE, also known as 3-Bromofuran-2,5-dione, is a pale red liquid with unique chemical properties. It is a compound that has found applications in various fields due to its ability to study reversible or permanent chemical modifications of proteins and peptides through the control of maleimide hydrolysis.

5926-51-2

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5926-51-2 Usage

Uses

Used in Research and Development:
BROMOMALEIC ANHYDRIDE is used as a research compound for studying the reversible or permanent chemical modification of proteins and peptides. This is particularly important in understanding the structure and function of these biomolecules, as well as their interactions with other cellular components.
Used in Pharmaceutical Industry:
BROMOMALEIC ANHYDRIDE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties allow for the development of new drugs with potential applications in treating a wide range of diseases and conditions.
Used in Chemical Modification of Biomolecules:
BROMOMALEIC ANHYDRIDE is used as a modifying agent for the chemical modification of proteins and peptides. This modification can enhance the stability, solubility, or biological activity of these biomolecules, making them more effective for various applications, such as drug delivery or enzyme catalysis.
Used in Material Science:
BROMOMALEIC ANHYDRIDE can be used as a component in the development of new materials with specific properties. Its chemical reactivity and ability to form covalent bonds with other molecules make it a valuable addition to the field of material science, where it can be used to create novel polymers, coatings, or other advanced materials with unique characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 5926-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5926-51:
(6*5)+(5*9)+(4*2)+(3*6)+(2*5)+(1*1)=112
112 % 10 = 2
So 5926-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C4HBrO3/c5-2-1-3(6)8-4(2)7/h1H

5926-51-2 Well-known Company Product Price

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  • Aldrich

  • (105023)  Bromomaleicanhydride  97%

  • 5926-51-2

  • 105023-10G

  • 857.61CNY

  • Detail
  • Aldrich

  • (105023)  Bromomaleicanhydride  97%

  • 5926-51-2

  • 105023-50G

  • 3,418.74CNY

  • Detail

5926-51-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Bromomaleic anhydride

1.2 Other means of identification

Product number -
Other names 3-bromofuran-2,5-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5926-51-2 SDS

5926-51-2Relevant academic research and scientific papers

A dinuclear iron(II) complex bearing multidentate pyridinyl ligand: Synthesis, characterization and its catalysis on the hydroxylation of aromatic compounds

Gu, Erxing,Zhong, Wei,Ma, Hongxia,Xu, Beibei,Wang, Hailong,Liu, Xiaoming

, p. 159 - 165 (2018/03/29)

A dinuclear iron(II) complex Fe2L2(μ2-Cl)2Cl2 (L = N,N-bis(pyridin-2-ylmethyl)prop-2-yn-1-amine) was prepared and fully characterized by UV–Vis spectroscopy, elemental analysis, electrochemical analysis and X-ray single crystal diffraction analysis. The catalytic activity of the complex was assessed for the hydroxylation of aromatic compounds by using aqueous H2O2 as an oxidant in acetonitrile. The catalytic system was applicable in a wide range of substrates including aromatic compounds with both electron-donating and electron-withdrawing substituents and showed moderate to good catalytic activity and selectivity in the oxidation reactions. Particularly, in the case of benzene the selectivity of phenol achieve to 74% with the reaction conversion of 24.8%.

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