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1659-68-3

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1659-68-3 Usage

Abbreviation

CDCA

Chemical structure

Cyclohexadiene ring with two carboxylic acid functional groups

Functional groups

Carboxylic acid

Usage

a. Monomer in the production of high-performance polymers
b. Production of polyimides
c. Production of polyester resins
d. Synthesis of pharmaceuticals
e. Synthesis of other organic compounds

Physical state

Colorless, crystalline solid

Melting point

High melting point (specific value not provided)

Solubility

Soluble in organic solvents such as ethanol and acetone

Applications

Wide range of uses in various sectors, including industrial chemical production

Importance

Versatile applications make it an important industrial chemical

Check Digit Verification of cas no

The CAS Registry Mumber 1659-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1659-68:
(6*1)+(5*6)+(4*5)+(3*9)+(2*6)+(1*8)=103
103 % 10 = 3
So 1659-68-3 is a valid CAS Registry Number.

1659-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexa-1,3-diene-1,4-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names Cyclohexa-1,3-dien-1,4-dicarbonsaeure

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:1659-68-3 SDS

1659-68-3Relevant articles and documents

Organometallic Compounds in Organic Synthesis. Part 14. Tricarbonyliron as Lateral Control Group in the Selective Alkaline Hydrolysis of some Cyclohexa-1,3-diene Carboxylic Esters

Bandara, B. M. Ratnayake,Birch, Arthur J.,Raverty, Warwick D.

, p. 1763 - 1770 (2007/10/02)

Alkaline hydrolyses of a number of methoxycarbonyl derivatives of cyclohexa-1,3-diene-Fe(CO)3 have been used as indices of steric and electronic effects on reactivities of the ester groups.A β-CO2Me or a 1-CO2Me group is resistant to hydrolysis for steric

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