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21676-88-0

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21676-88-0 Usage

General Description

4-Phenylthiophene-2-Carboxylic Acid is an organic compound consisting of a thiophene moiety substituted at the 2-position by a carboxylic acid function and at the 4-position by a phenyl group. Its molecular formula is C12H10O2S. This chemical has an aromatic ring exhibiting delocalized pi electron systems, making it stable and inert to many chemical reactions. Despite its stability, however, it can undergo reactions under certain conditions, which entail the addition or substitution at its reactive sites. Typically, this chemical is used as a chemical intermediate or a building block during the synthesis of various other compounds, including pharmaceuticals. However, like many chemicals, it can potentially affect human health and the environment if mishandled, making it necessary to handle it with utmost care and in compliance with standard safety procedures. Regular safety evaluation and valid certifications are also required for its manufacturing and usage.

Check Digit Verification of cas no

The CAS Registry Mumber 21676-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,7 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21676-88:
(7*2)+(6*1)+(5*6)+(4*7)+(3*6)+(2*8)+(1*8)=120
120 % 10 = 0
So 21676-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2S/c12-11(13)10-6-9(7-14-10)8-4-2-1-3-5-8/h1-7H,(H,12,13)

21676-88-0 Well-known Company Product Price

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  • Aldrich

  • (686905)  4-Phenylthiophene-2-carboxylicacid  97%

  • 21676-88-0

  • 686905-1G

  • 1,078.74CNY

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21676-88-0SDS

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 4-PHENYLTHIOPHENE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 2-Carboxy-4-phenylthiophen

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:21676-88-0 SDS

21676-88-0Relevant articles and documents

Redox-Neutral Photocatalytic C?H Carboxylation of Arenes and Styrenes with CO2

Bergonzini, Giulia,Brandt, Peter,Fricke, Florian,Johansson, Magnus J.,K?nig, Burkhard,Schmalzbauer, Matthias,Svejstrup, Thomas D.

, p. 2658 - 2672 (2020/10/07)

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Furan- and thiophene-2-carbonyl amino acid derivatives activate hypoxia-inducible factor via inhibition of factor inhibiting hypoxia-inducible factor-1

Kawaguchi, Shin-ichi,Gonda, Yuhei,Yamamoto, Takuya,Sato, Yuki,Shinohara, Hiroyuki,Kobiki, Yohsuke,Ichimura, Atsuhiko,Dan, Takashi,Sonoda, Motohiro,Miyata, Toshio,Ogawa, Akiya,Tsujita, Tadayuki

, (2018/04/17)

Induction of a series of anti-hypoxic proteins protects cells during exposure to hypoxic conditions. Hypoxia-inducible factor-α (HIF-α) is a major transcription factor that orchestrates this protective effect. To activate HIF exogenously, without exposing

3-alkyl or aryl thiophenes from malonaldehyde derivatives

Kirsch,Prim

, p. 1721 - 1726 (2007/10/02)

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