5693-09-4 Usage
Physical form
White powder, which describes the appearance of the compound.
Chemical structure
Consists of two benzene rings attached to a butanedioic acid molecule, which provides information about the compound's chemical structure.
Derivative of succinic acid
Indicates that the compound is derived from succinic acid, which is a key information for understanding its chemical properties.
Chelating agent
Used in the metal finishing industry for the removal of excess metal ions from plating solutions, which highlights its industrial applications.
Medicinal use
Has potential as an inhibitor of type II collagen-induced arthritis, which indicates its potential use in the pharmaceutical industry.
Industrial and medicinal uses
Due to its chelating and inhibitory properties, the compound has various applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 5693-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5693-09:
(6*5)+(5*6)+(4*9)+(3*3)+(2*0)+(1*9)=114
114 % 10 = 4
So 5693-09-4 is a valid CAS Registry Number.
5693-09-4Relevant academic research and scientific papers
Triflic Acid Mediated Cyclization of Unsymmetrical N -Phenethyl- and N -(3-Indolylethyl)succinimides: Regio- and Diastereoselective Synthesis of Substituted Pyrroloisoquinolinones and Indolizino-indolones
Selvakumar, Jayaraman,Mangalaraj, Selvaraj,Achari, Kamsali Murali Mohan,Mukund, Krishna,Ramanathan, Chinnasamy Ramaraj
supporting information, p. 1053 - 1064 (2017/02/24)
The regio and diastereoselective synthesis of 1 or 2 alkyl-substituted pyrroloisoquinolinones and indolizinoindolones by triflic acid mediated cyclization via an electrophilic activation of unsymmetrical succinimide carbonyl groups followed by the reducti
