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1,4-Benzenedicarboxylic acid, 2,5-bis(acetylamino)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

657412-63-0

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657412-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 657412-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,7,4,1 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 657412-63:
(8*6)+(7*5)+(6*7)+(5*4)+(4*1)+(3*2)+(2*6)+(1*3)=170
170 % 10 = 0
So 657412-63-0 is a valid CAS Registry Number.

657412-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2,5-diacetamidobenzene-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2.5-Bis-acetamino-terephthalsaeure-diaethylester

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:657412-63-0 SDS

657412-63-0Relevant academic research and scientific papers

Hydrogen Bond-Induced Rigid Oligoanthranilamide Ribbons That Are Planar and Straight

Wu, Zong-Quan,Jiang, Xi-Kui,Zhu, Shi-Zheng,Li, Zhan-Ting

, p. 229 - 232 (2007/10/03)

(Matrix presented) A new series of oligoanthranilamides has been synthesized starting from suitably modified p-phenylenediamine and p-phthalic acid derivatives. Due to strong intramolecular three-center hydrogen bonds, the new oligomers self-assemble into highly stable straight and planar molecular ribbons, which have been characterized by X-ray crystallography and 1H NMR, IR, and UV-vis spectroscopy.

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