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1,3-Benzenedicarboxylic acid, 2-(carboxycarbonyl)-, also known as 2-(oxalyl)terephthalic acid, is an organic compound with the chemical formula C10H6O8. It is a derivative of terephthalic acid, featuring an additional oxalyl group (-CO-CO-) attached to the 2-position of the benzene ring. 1,3-Benzenedicarboxylicacid, 2-(carboxycarbonyl)- is a white crystalline solid and is used as an intermediate in the synthesis of various polymers, dyes, and pharmaceuticals. Its chemical structure consists of a benzene ring with two carboxylic acid groups at the 1 and 3 positions and an oxalyl group at the 2 position, which contributes to its reactivity and versatility in chemical synthesis.

3112-43-4

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3112-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3112-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3112-43:
(6*3)+(5*1)+(4*1)+(3*2)+(2*4)+(1*3)=44
44 % 10 = 4
So 3112-43-4 is a valid CAS Registry Number.

3112-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxalobenzene-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2-hydroxyoxalyl-isophthalic acid

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:3112-43-4 SDS

3112-43-4Relevant academic research and scientific papers

SYNTHESE PHOTOCHIMIQUE D'HYDROCARBURES POLYCYCLIQUES AROMATIQUES ET ETUDE EN RMN-1H DES PROTONS DE BAIE. EFFECTS DE SOLVANT SPECIFIQUES ET EFFECTS NUCLEAIRES OVERHAUSER.

Brison, Jean,Bakker, Claude de,Defay, Nicole,Geerts-Evrard, France,Marchant, Marie-Jeanne,Martin, Richard H.

, p. 901 - 912 (2007/10/02)

"Photochemical synthesis of polycyclic aromatic hydrocarbons and NMR-1H study of bay protons.Specific solvent effects and nuclear Overhauser effects".Dinaphthoanthracene (4a),9-bromo-dinaphthoanthracene (4b), 9-methyldinaphthoanthracene (4c), benzonaphthochrysene (7), benzonaphthoanthracene (3), naphthochrysene (9) and dibenzonaphthochrysene (12) have been synthesized by the photocyclodehydrogenation of 1,2-diarylethylenes (5,8) and bis (arylvinyl)arenes (6,10).The NMR study has been mainly focused on the bay protons involved in specific solvent effects Table 4) and nuclear Overhauser effects (Table 5).

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