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19163-24-7

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  • BEST PRICE/5-Phenylthiophene-2-carboxylic acid CAS NO.19163-24-7

    Cas No: 19163-24-7

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19163-24-7 Usage

General Description

5-Phenylthiophene-2-carboxylic acid is a chemical compound with the molecular formula C11H8O2S. It is a carboxylic acid derivative of phenylthiophene, which is a heterocyclic compound containing a thiophene ring with a phenyl group attached. 5-Phenylthiophene-2-carboxylic acid has potential applications in organic synthesis and material science. It is known for its aromatic and electron-rich nature, making it useful as a building block for the synthesis of various organic molecules. Additionally, it has been studied for its potential pharmaceutical properties and its role in the development of new drugs. Overall, 5-Phenylthiophene-2-carboxylic acid is a versatile and valuable chemical compound with diverse applications in various fields of science and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 19163-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19163-24:
(7*1)+(6*9)+(5*1)+(4*6)+(3*3)+(2*2)+(1*4)=107
107 % 10 = 7
So 19163-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3N2/c9-8(10,11)6-1-2-7(3-4-12)13-5-6/h1-2,5H,3H2

19163-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Phenyl-2-thiophenecarboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Phenylthiophene-2-carboxylic acid

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 -
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More Details:19163-24-7 SDS

19163-24-7Relevant articles and documents

Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd-C Bonds and Suzuki-Miyaura Reactions

Asensio, Juan M.,Andrés, Román,Gómez-Sal, Pilar,De Jesús, Ernesto

, p. 4191 - 4201 (2017)

The synthesis of water-soluble η3-allyl Pd(II) complexes containing sulfonated N-heterocyclic carbene (NHC) ligands of general formula [Pd(NHC)n(η3-allyl)Cl2-n] is reported (n = 1 (1) or 2 (8)). Monocarbene complexes were obtained with the most sterically hindered NHC ligands, and biscarbenes with the less sterically hindered NHCs. The behavior of the isolated complexes in water under acidic, neutral, or alkaline conditions has been studied. The complexes are rather stable in water under neutral or alkaline conditions, although displacement of the chlorido ligand by water or hydroxide occurs under these conditions. In acidic media, Pd-NHC bonds are protolysed, and it is especially noteworthy that this protolysis occurs preferentially to that of the Pd-allyl bonds in the case of the complexes with the less-sterically hindered NHC ligands. This behavior contrasts with that observed in dimethyl sulfoxide (dmso), where the Pd-allyl bonds are selectively broken upon treatment with Br?nsted acids. In addition, Pd-NHC bond breaking was promoted by the addition of a strong σ-donor ligand such as cyanide. Complex 1a is an active catalyst for the Suzuki-Miyaura cross-coupling of water-soluble aryl chlorides in neat water under moderate conditions (typically, 0.5 mol % Pd and 60 °C).

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Chakrabarti,Chapman

, p. 914,918,919 (1970)

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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.

supporting information, 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

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