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2-Thiophenecarboxylic acid, 3-amino-4-cyano-5-(phenylamino)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59615-90-6

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59615-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59615-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,1 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59615-90:
(7*5)+(6*9)+(5*6)+(4*1)+(3*5)+(2*9)+(1*0)=156
156 % 10 = 6
So 59615-90-6 is a valid CAS Registry Number.

59615-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-cyano-5-phenylamino-thiophene-2-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-amino-4-cyano-5-phenylaminothiophene-2-carboxylic acid ethyl ester

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:59615-90-6 SDS

59615-90-6Relevant academic research and scientific papers

NBS-mediated sequential one-pot synthesis of multifunctionalized thiazoles and thiophenes from 1,3-dicarbonyl compounds and mercaptonitrile salts

Luo, Laichun,Meng, Lanlan,Sun, Qi,Ge, Zemei,Li, Runtao

supporting information, p. 259 - 263 (2014/01/06)

A NBS-mediated sequential one-pot synthesis of multifunctionalized thiazoles and thiophenes from 1,3-dicarbonyl compounds and mercaptonitrile salts has been developed under mild conditions. This transformation involves sequential bromination/SN

Preparation of thieno[2,3-b]pyrroles starting from ketene-N,S-acetals

Sommen, Geoffroy,Comel, Alain,Kirsch, Gilbert

, p. 1557 - 1564 (2007/10/03)

Thieno[2,3-b]pyrroles 4 can easily be synthesised in two different ways by using phenyl isothiocyanate and activated methylene compounds. The priority of the formation of the thiophene or pyrrole ring is investigated.

An improved method for the synthesis of aminothiophenes precursors of thieno[2,3-b]pyrrole

Sommen, Geoffroy,Comel, Alain,Kirsch, Gilbert

, p. 257 - 259 (2007/10/03)

Thiophenes 2 can easily be synthesized in two steps by using phenyl isothiocyanate and activated methylene compounds.

An easy access to variously substituted thieno[2,3-b]pyrroles by using isothiocyanates

Sommen,Comel,Kirsch

, p. 1731 - 1734 (2007/10/03)

Thieno[2,3-b]pyrroles 2 can easily be synthesised in two steps by using isothiocyanates and activated methylene compounds.

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