7126-27-4 Usage
Description
3-[2-(3-carboxyprop-2-enoylamino)ethylcarbamoyl]prop-2-enoic acid is a complex chemical compound derived from prop-2-enoic acid. It features a prop-2-enoic acid backbone with additional functional groups and side chains, including carboxylic and carbamoyl groups, as well as an ethylamino side chain connected to the carbamoyl group. This versatile molecule has a unique structure that allows it to participate in various chemical reactions and applications.
Uses
Used in Chemical Synthesis:
3-[2-(3-carboxyprop-2-enoylamino)ethylcarbamoyl]prop-2-enoic acid is used as a building block in chemical synthesis for creating new compounds with specific properties. Its functional groups and side chains enable it to react with other molecules, making it a valuable component in the development of novel materials and pharmaceuticals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-[2-(3-carboxyprop-2-enoylamino)ethylcarbamoyl]prop-2-enoic acid is used as an active pharmaceutical ingredient (API) for the development of new drugs. Its unique structure and functional groups allow it to interact with biological targets, potentially leading to the discovery of new therapeutic agents.
Used in Material Science:
3-[2-(3-carboxyprop-2-enoylamino)ethylcarbamoyl]prop-2-enoic acid is used in material science for the development of advanced materials with specific properties. Its ability to participate in chemical reactions and form covalent bonds with other molecules makes it a promising candidate for creating new materials with tailored characteristics for various applications.
Used in Research and Development:
In research and development, 3-[2-(3-carboxyprop-2-enoylamino)ethylcarbamoyl]prop-2-enoic acid is used as a starting material for exploring new chemical reactions and understanding the behavior of complex molecules. Its unique structure provides opportunities for scientists to investigate its properties and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 7126-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7126-27:
(6*7)+(5*1)+(4*2)+(3*6)+(2*2)+(1*7)=84
84 % 10 = 4
So 7126-27-4 is a valid CAS Registry Number.
7126-27-4Relevant articles and documents
Hydrolytic degradation of N,N′-ethylenedimaleimide: Crystal structures of key intermediates and proposed mechanisms
Tan, Xue-Jie,Cheng, Shuang-Shuang,Shi, Yan,Xing, Dian-Xiang,Liu, Yun,Li, Hui,Feng, Wen-Quan,Yang, Jian-Bo
, p. 514 - 521 (2016/07/21)
Maleimide groups are used extensively in bioconjugation reactions, but limited mechanistic studies are available regarding their hydrolysis reactions. In this paper, five single-crystal structures related with the reaction of four-step hydrolytic degradation of N,N′-ethylenedimaleimide have been investigated. On the basis of experimental results, the reaction mechanisms without or with water catalysis are proposed, which could provide some enlightenment into the study of similar hydrolytic degradations.
Synthesis and characterization of cobalt(II), nickel(II), copper(II) and palladium(II) complexes of polydentate ligands
Swamy, G. Bala,Ravinder, V.,Swamy, S. J.
, p. 589 - 593 (2007/10/02)
A few complexes of Co(II), Ni(II), Cu(II) and Pd(II) with a tetradentate ligand N,N'-ethylene-bis-(3-carboxypropenamide) and a bidentate ligand benz--2-carboxymethyl-1,3,4-thiolactam have been synthesised and characterized by elemental analyses, conductance, thermal, magnetic and IR, NMR and electronic spectral studies.
