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36978-40-2

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36978-40-2 Usage

Structure

A derivative of biphenyl with four carboxylic acid groups attached to the aromatic rings

Application

Used in the production of functional materials such as liquid crystals and metal-organic frameworks

Thermal stability

Known for its high thermal stability

Potential applications

Electronic devices and optoelectronic materials

Coordination chemistry

Studied for its potential use as a chelating ligand

Surface properties

Ability to form self-assembled monolayers on surfaces

Check Digit Verification of cas no

The CAS Registry Mumber 36978-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36978-40:
(7*3)+(6*6)+(5*9)+(4*7)+(3*8)+(2*4)+(1*0)=162
162 % 10 = 2
So 36978-40-2 is a valid CAS Registry Number.

36978-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name biphenyl-2,3,3',4-tetracarboxylic acid

1.2 Other means of identification

Product number -
Other names 2,3,3',4'-biphenyltetracarboxylic 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:36978-40-2 SDS

36978-40-2Relevant articles and documents

Method for preparing biphenyldianhydride isomer by ultrasonic-assisted catalytic coupling

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Paragraph 0028-0030, (2021/11/06)

The invention discloses a method for preparing biphenyldianhydride isomers through ultrasonic-assisted catalytic coupling. The main contents include a mixture of a nickel salt catalyst and zinc as a reducing agent, 2-THF used as a solvent, an aryl (or methyl) N - chloronaphthalimide and -4 - propyl (or isopropyl) N - chlorodifluoroimide, under -3 - by means of an ultrasonic-assisted catalytic coupling reaction 60 - 100 °C 0.5 - 3 hours. The separation and purification of the three biphenyltetracarboxylic acid isomers are realized by using different solubility parameters, and the biphenyldianhydride isomer pure product is finally obtained. The invention is characterized in that a simple method for separating the three biphenyltetracarboxylic acid isomers is established, the problem of difficulty in separation of the three biphenyl dianhydride mixtures is solved, and 3,4 - biphenyl dianhydride ’ with an asymmetric structure is obtained at lower cost.

Process for production of 2, 3, 3', 4'-biphenyltetracarboxylic dianhydride

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Page/Page column 6, (2010/11/24)

A process for producing 2,3,3′,4′-biphenyltetracarboxylic dianhydride (a-BPDA), comprising dehydrating 2,3,3′,4′-biphenyltetracarboxylic acid in an inert gas atmosphere under heating at 180 to 195° C is disclosed. This process produces high-purity a-BPDA which is suitable for production of a polyimide.

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