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80691-81-2

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80691-81-2 Usage

General Description

2,5-Diaminothiophene-3,4-dicarboxylic acid diethyl ester is a chemical compound usually used in the field of organic chemistry. It is utilized as an intermediate in the synthesis of various compounds due to its distinct structural properties: two amino groups (-NH2) on the thiophene ring, and two ester-containing carboxylic acids. These groups allow it to participate in a variety of chemical reactions. 2,5-Diaminothiophene-3,4-dicarboxylic acid diethyl ester is often subjected to further transformations to result in new molecules with potential applications in pharmaceuticals, polymers and dyes production.

Check Digit Verification of cas no

The CAS Registry Mumber 80691-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,9 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80691-81:
(7*8)+(6*0)+(5*6)+(4*9)+(3*1)+(2*8)+(1*1)=142
142 % 10 = 2
So 80691-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O4S/c1-3-15-9(13)5-6(10(14)16-4-2)8(12)17-7(5)11/h3-4,11-12H2,1-2H3

80691-81-2SDS

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 diethyl 2,5-diaminothiophene-3,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,5-Diaminothiophen-3,4-dicarbonsaeurediethylester

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:80691-81-2 SDS

80691-81-2Relevant articles and documents

Optimized synthesis and simple purification of 2,5-diamino-thiophene-3,4- dicarboxylic acid diethyl ester

Bourgeaux, Marie,Vomscheid, Sophie,Skene

, p. 3551 - 3558 (2007)

A stable diamino thiophene was synthesized in high purity with a three-fold increase in yield over previous reports via simple crystallization using inexpensive reagents. Copyright Taylor & Francis Group, LLC.

Discovery of diethyl 2,5-diaminothiophene-3,4-dicarboxylate derivatives as potent anticancer and antimicrobial agents and screening of anti-diabetic activity: Synthesis and in vitro biological evaluation. Part 1

Bozorov, Khurshed,Ma, Hai-Rong,Zhao, Jiang-Yu,Zhao, Hai-Qing,Chen, Hua,Bobakulov, Khayrulla,Xin, Xue-Lei,Elmuradov, Burkhon,Shakhidoyatov, Khusnutdin,Aisa, Haji A.

, p. 739 - 745 (2014)

Series of diethyl 2,5-diaminothiophene-3,4-dicarboxylate (DDTD) derivatives: azomethines of DDTD (2a el) have been synthesized and screened for their anticancer, antimicrobial and anti-diabetic activities. The novel synthesized compounds were characterize

A 2,5-diamino -3,4-thiophene dicarboxylate ethyl derivatives preparation method and use

-

Paragraph 0026-0027, (2017/02/24)

The invention relates to a preparation method and application of ethyl 2,5-diamido-3,4-thienyldicarboxylate derivatives. Sulfur and ethyl cyanoacetate used as raw materials are condensed with substitution benzaldehyde or arylheterocyclo aldehyde under the

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