77280-58-1 Usage
Uses
Used in Chemical Synthesis:
4,4'-Bis(MaleoylaMino)azobenzene is used as a bifunctional crosslinker for directed modification of proteins and other crosslinking processes. Its ability to form covalent bonds with target molecules allows for the creation of new materials with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-Bis(MaleoylaMino)azobenzene is used as a key intermediate in the synthesis of drug candidates. Its unique reactivity and crosslinking capabilities enable the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Materials Science:
4,4'-Bis(MaleoylaMino)azobenzene is employed as a building block in the design and synthesis of advanced materials. Its ability to form stable crosslinks with various substrates contributes to the development of materials with enhanced mechanical, thermal, and chemical properties.
Used in Research and Development:
In research and development, 4,4'-Bis(MaleoylaMino)azobenzene serves as a valuable tool for studying the fundamental properties of azobenzene derivatives and their interactions with other molecules. This knowledge can be applied to the design of new materials and the optimization of existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 77280-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,8 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77280-58:
(7*7)+(6*7)+(5*2)+(4*8)+(3*0)+(2*5)+(1*8)=151
151 % 10 = 1
So 77280-58-1 is a valid CAS Registry Number.
77280-58-1Relevant academic research and scientific papers
New azobenzene derivatives for directed modification of proteins
Hien, Le Thi,Schierling,Ryazanova,Zatsepin,Volkov,Kubareva,Velichko,Pingoud,Oretskaya
experimental part, p. 549 - 555 (2010/08/22)
Derivatives of azobenzene which contained a maleimide group in one of the benzene rings (for binding to a protein cysteine residue) and maleimide, hydroxyl, or carboxyl substitutes in another benzene ring were synthesized. The reactivity of these compound