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2060-55-1

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2060-55-1 Usage

General Description

2,2'-Bithiophene-5-carboxylic acid is an organic chemical compound that primarily falls under the category of heterocyclic compounds, more specifically, the thiophene group. As the name suggests, it incorporates two thiophene rings linked at the 2-position, with a carboxylic acid functional group attached to the 5-position of one of the rings. The carboxylic acid functional group contributes to its acidic nature. Known for its biological activity, it is often used in pharmaceuticals and serves as a useful synthetic intermediate for numerous organic reactions. Other applications include its use in the production of polymers and optoelectronic materials.

Check Digit Verification of cas no

The CAS Registry Mumber 2060-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2060-55:
(6*2)+(5*0)+(4*6)+(3*0)+(2*5)+(1*5)=51
51 % 10 = 1
So 2060-55-1 is a valid CAS Registry Number.

2060-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-thiophen-2-ylthiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,2'-Bithiophene-5-CA

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:2060-55-1 SDS

2060-55-1Relevant articles and documents

Chiral aggregates of α,ω-disubstituted sexithiophenes in protic and aqueous media [10]

Kilbinger,Schenning,Goldoni,Feast,Meijer

, p. 1820 - 1821 (2000)

-

Structural, spectroscopic, and computational studies of [2,2′-bithiophene]-5-carboxylic acid

Einkauf, Jeffrey D.,Mathivathanan, Logesh,De Lill, Daniel T.

, p. 33 - 39 (2015/10/28)

The crystal structure of [2,2′-bithiophene]-5-carboxylic acid was obtained from in-situ decarboxylation of [2,2′-bithiophene]-5,5′-dicarboxylic acid during solvothermal treatment. UV-Vis absorption and fluorescence spectroscopies were conducted in solution and solid-state on these two molecules as well as the precursor, 2,2′-bithiophene. These molecules were modeled using DFT level of theory to explain the observed structural features and spectroscopy.

Amide compounds

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Page column 16, (2010/02/07)

The present invention is a compound and pharmaceutical composition comprising a compound of formula (I): wherein R1is a 4-(lower) alkyl-imidazol-1-yl or a 4,5-di(lower) alkyl-imidazol-1-yl group, R2is a hydrogen atom or a lower alkyl

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