61960-57-4 Usage
Description
3-Maleimidobenzoic acid chloride is a white solid chemical compound derived from maleic anhydride and 3-aminobenzoic acid. It is used as a reagent in organic synthesis and biochemical research, and serves as an important intermediate in the production of dyes, pharmaceuticals, and as a crosslinking agent in polymer chemistry. This versatile chemical finds applications in the fields of chemistry, materials science, and biotechnology.
Uses
Used in Chemical Synthesis:
3-Maleimidobenzoic acid chloride is used as a reagent in organic synthesis for its ability to form stable maleimide rings, which are useful in the creation of various chemical compounds.
Used in Biochemical Research:
In biochemical research, 3-maleimidobenzoic acid chloride is used as a modifying agent to study the properties and functions of biomolecules, taking advantage of its reactive maleimide group.
Used in Pharmaceutical Production:
3-Maleimidobenzoic acid chloride is used as an important intermediate in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Dye Manufacturing:
3-MALEIMIDOBENZOIC ACID CHLORIDE is utilized in the manufacturing of dyes, where its chemical properties allow for the creation of a wide range of colorants for various applications.
Used in Polymer Chemistry:
3-Maleimidobenzoic acid chloride is used as a crosslinking agent in polymer chemistry, enabling the formation of networks and improving the mechanical properties of polymeric materials.
Used in Materials Science:
In the field of materials science, 3-maleimidobenzoic acid chloride is employed to develop new materials with enhanced properties, such as improved stability and reactivity, by incorporating its unique chemical structure.
Check Digit Verification of cas no
The CAS Registry Mumber 61960-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61960-57:
(7*6)+(6*1)+(5*9)+(4*6)+(3*0)+(2*5)+(1*7)=134
134 % 10 = 4
So 61960-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H6ClNO3/c12-11(16)7-2-1-3-8(6-7)13-9(14)4-5-10(13)15/h1-6H
61960-57-4Relevant articles and documents
Synthesis of benzene-1,4-diylbis(oxyethane-2,1-diyl) bis[(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoates]
Kolyamshin,Kuz'min,Ignat'ev,Rogozhina,Kol'tsov
, p. 901 - 902 (2015/08/06)
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Thermal studies of bismaleimides. II Bismaleimides with ester units
Sava, Miticǎ,Gǎinǎ, Constantin,Gǎinǎ, Viorica
, p. 1167 - 1173 (2007/10/03)
Bismaleimides containing ester groups in the backbone were synthesized from 3(4)-maleimido benzoic acid chloride with varies diphenols. These bismaleimides are characterized by DSC studies, thermogravimetric analysis and isothermal gravimetric analysis (IGA). The thermal properties of these compounds were compared.
Synthesis of New Bifunctional Maleimide Compounds for the Preparation of Chemoimmunoconjugates
Beyer,Krüger,Schumacher,Unger,Kratz
, p. 91 - 102 (2007/10/03)
Bifunctional maleimide compounds are suitable for binding small molecules to carrier proteins in that they bind to the sulfhydryl group of proteins through the double bond of the maleimide group and to molecules of low molecular weight (e.g. anticancer drugs) through a functional group X. 18 maleimide compounds of the general formula Maleimid-R-X (R = phenylene, benzyl-, methylene-, ethylene, or a m-benzoylethylamide group and X = hydroxy-, amino-, hydrazino-, carboxylic acid-, carboxylic anhydride-, carboxylic acid chloride-, carboxylic acid hydrazide-, oxycarbonylchloride-, aldehyde, keto-, or p-toluenesulfonate-group) were synthesized and characterized through 1H- and 13C-NMR-spectroscopy, elemental analysis, and mass spectrometry.
