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1,3-Benzenedicarboxylic acid, 4,6-bis[(phenylamino)carbonyl]-, also known as 4,6-Bis(phenylaminocarbonyl)phthalic acid, is a complex organic compound with the chemical formula C20H14N2O4. It is a derivative of phthalic acid, where two of the hydrogen atoms on the benzene ring are replaced by phenylaminocarbonyl groups. 1,3-Benzenedicarboxylic acid, 4,6-bis[(phenylamino)carbonyl]- is characterized by its ability to form various salts and esters, which are used in the synthesis of dyes, pharmaceuticals, and other specialty chemicals. Its molecular structure features a central benzene ring with two carboxylic acid groups at the 1 and 3 positions, and two phenylaminocarbonyl groups attached at the 4 and 6 positions, creating a symmetrical and conjugated system that can participate in various chemical reactions.

60684-14-2

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60684-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60684-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,8 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60684-14:
(7*6)+(6*0)+(5*6)+(4*8)+(3*4)+(2*1)+(1*4)=122
122 % 10 = 2
So 60684-14-2 is a valid CAS Registry Number.

60684-14-2SDS

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 4,6-bis(phenylcarbamoyl)benzene-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names pyromellitodianilic 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:60684-14-2 SDS

60684-14-2Downstream Products

60684-14-2Relevant academic research and scientific papers

Bronsted base-assisted boronic acid catalysis for the dehydrative intramolecular condensation of dicarboxylic acids

Sakakura, Akira,Ohkubo, Takuro,Yamashita, Risa,Akakura, Matsujiro,Ishihara, Kazuaki

supporting information; experimental part, p. 892 - 895 (2011/05/02)

Bronsted base-assisted boronic acid catalysis for the dehydrative self-condensation of carboxylic acids is described. Arylboronic acid bearing bulky (N,N-dialkylamino)methyl groups at the 2,6-positions can catalyze the intramolecular dehydrative condensation of di-and tetracarboxylic acids. This is the first successful method for the catalytic dehydrative self-condensation of carboxylic acids.(Figure Presented)

METHOD FOR PRODUCING CARBOXYLIC ANHYDRIDE AND ARYLBORONIC ACID COMPOUND

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Page/Page column 13, (2012/01/13)

When phthalic acid is heated in heptane under azeotropic reflux conditions in the presence of a catalytic amount of an arylboronic acid compound (such as 2,6-(diisopropylaminomethyl)phenylboronic acid or 2,6-bis(diisopropylaminomethyl)phenylboronic acid), phthalic anhydride is obtained in high yield.

ISOMERISM IN COMPLEXES OF PYROMELLITIC ACID DIANILIDE WITH APROTIC POLAR SOLVENTS

Denisov, V. M.,Shibaev, L. A.,Dauengauer, S. A.,Sazanov, Yu. N.,Kol'tsov, A. I.

, p. 1141 - 1145 (2007/10/02)

A study has been carried out of isomerism in complexes of pyromellitic acid dianilide with aprotic polar solvents, and crystalline complexes have been isolated which contain only the paraisomer of the original acid.It has been shown to be possible to convert one isomeric complex into another in solution at moderate temperatures.

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