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5693-09-4

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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.

5693-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzhydrylidenebutanedioic acid

1.2 Other means of identification

Product number -
Other names Butanedioic acid, (diphenylmethylene)-

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:5693-09-4 SDS

5693-09-4Relevant articles and documents

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

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