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29886-64-4

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29886-64-4 Usage

General Description

4-(3-thienyl)benzoic acid is a chemical compound with the formula C13H10O2. It is a derivative of benzoic acid, with a thienyl group attached at the 4-position. 4-(3-THIENYL)BENZOIC ACID is commonly used in organic synthesis and pharmaceutical research due to its potential as a building block for various bioactive molecules. It has been studied for its potential medicinal properties, including anti-inflammatory and anti-cancer effects. Additionally, 4-(3-thienyl)benzoic acid has been investigated for its potential use as a fluorescent probe for detecting RNA secondary structures. Its unique structure and potential biological activities make it an interesting target for further research and development in the fields of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 29886-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29886-64:
(7*2)+(6*9)+(5*8)+(4*8)+(3*6)+(2*6)+(1*4)=174
174 % 10 = 4
So 29886-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2S/c12-11(13)9-3-1-8(2-4-9)10-5-6-14-7-10/h1-7H,(H,12,13)

29886-64-4SDS

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 4-thiophen-3-ylbenzoic acid

1.2 Other means of identification

Product number -
Other names F9995-0348

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:29886-64-4 SDS

29886-64-4Relevant articles and documents

CoIII-Catalyzed Isonitrile Insertion/Acyl Group Migration Between C?H and N?H bonds of Arylamides

Kalsi, Deepti,Barsu, Nagaraju,Sundararaju, Basker

supporting information, p. 2360 - 2364 (2018/02/22)

A general efficient and site-selective cobalt-catalyzed insertion of isonitrile into C?H and N?H bonds of arylamides through C?H bond activation and alcohol assisted intramolecular trans-amidation is demonstrated. This straightforward approach overcomes the limitation by the presence of strongly chelating groups. Isolation of CoIII-isonitrile complex B has been achieved for the first time to understand the reaction mechanism.

Structural modifications of salicylates: Inhibitors of human CD81-receptor HCV-E2 interaction

Holzer, Marcel,Ziegler, Sigrid,Neugebauer, Alexander,Kronenberger, Bernd,Klein, Christian D.,Hartmann, Rolf W.

experimental part, p. 478 - 484 (2009/04/04)

Starting point of the present paper was the result of a virtual screening using the open conformation of the large extracellular loop (LEL) of the CD81-receptor (crystal structure: PDB-ID: 1G8Q). After benzyl salicylate had been experimentally validated to be a moderate inhibitor of the CD81-LEL-HCV-E2 interaction, further optimization was performed and heterocyclic-substituted benzyl salicylate derivatives were synthesized. The compounds were tested for their ability to inhibit the interaction of a fluorescence-labeled antibody to CD81-LEL using HUH7.5 cells. No compound showed an increase concerning the inhibition of the protein-protein interaction compared to benzyl salicylate.

A novel anthracenyl tagged protecting group for "phase-switching" applications in parallel synthesis

Li, Xin,Abell, Chris,Ladlow, Mark

, p. 4189 - 4194 (2007/10/03)

A new "phase-switching" protecting group 1 that facilitates the parallel synthesis of carboxylic acids, esters, and carboxamides is described. Its use permits chemistries to be performed in solution, which may be conveniently monitored with conventional a

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