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6-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid is a chemical compound characterized by its molecular formula C10H5F3O2S. It is a carboxylic acid derivative of benzo[b]thiophene, a heterocyclic compound featuring a thiophene ring fused to a benzene ring. The distinctive trifluoromethyl group attached to the benzo[b]thiophene core endows it with unique properties, making it a valuable compound in pharmaceuticals and materials science. Its potential applications in the synthesis of pharmaceutical agents and as a building block for organic synthesis highlight its significance in medicinal chemistry and drug discovery.

142329-22-4

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142329-22-4 Usage

Uses

Used in Pharmaceutical Synthesis:
6-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid is utilized as a key intermediate in the synthesis of various pharmaceutical agents. Its unique structure and properties contribute to the development of new drugs with improved therapeutic effects.
Used in Organic Synthesis:
As a building block for organic synthesis, 6-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid is employed in the creation of complex organic molecules. Its presence in these molecules can enhance their reactivity, stability, and other desirable properties.
Used in Medicinal Chemistry Research:
6-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid is an interesting target for research in the field of medicinal chemistry. Its unique structure allows for the exploration of new chemical reactions and the development of novel therapeutic agents.
Used in Drug Discovery:
In the realm of drug discovery, 6-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid plays a crucial role. Its unique properties make it a promising candidate for the development of new drugs with potential applications in various therapeutic areas.
Used in Materials Science:
6-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid also finds applications in materials science, where its unique structure and properties can be leveraged to develop new materials with specific characteristics for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 142329-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,3,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142329-22:
(8*1)+(7*4)+(6*2)+(5*3)+(4*2)+(3*9)+(2*2)+(1*2)=104
104 % 10 = 4
So 142329-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H5F3O2S/c11-10(12,13)6-2-1-5-3-8(9(14)15)16-7(5)4-6/h1-4H,(H,14,15)

142329-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(trifluoromethyl)-1-benzothiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Benzo[b]thiophene-2-carboxylicacid,6-(trifluoromethyl)

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:142329-22-4 SDS

142329-22-4Downstream Products

142329-22-4Relevant articles and documents

Design, synthesis, and biological activity evaluation of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives as broad-spectrum antifungal agents

Zhao, Liyu,Sun, Yin,Yin, Wenbo,Tian, Linfeng,Sun, Nannan,Zheng, Yang,Zhang, Chu,Zhao, Shizhen,Su, Xin,Zhao, Dongmei,Cheng, Maosheng

, (2021/11/22)

To discover antifungal compounds with broad-spectrum and stable metabolism, a series of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives was designed and synthesized. Compounds A30-A34 exhibited excellent broad-spectrum antifungal activity against Candida albicans with MIC values in the range of 0.03–0.5 μg/mL, and against Cryptococcus neoformans and Aspergillus fumigatus with MIC values in the range of 0.25–2 μg/mL. In addition, compounds A31 and A33 showed high metabolic stability in human liver microsomes in vitro, with the half-life of 80.5 min and 69.4 min, respectively. Moreover, compounds A31 and A33 showed weak or almost no inhibitory effect on the CYP3A4 and CYP2D6. The pharmacokinetic evaluation in SD rats showed that compound A31 had suitable pharmacokinetic properties and was worthy of further study.

Amide-Amine Replacement in Indole-2-carboxamides Yields Potent Mycobactericidal Agents with Improved Water Solubility

Tan, Yu Jia,Li, Ming,Gunawan, Gregory Adrian,Nyantakyi, Samuel Agyei,Dick, Thomas,Go, Mei-Lin,Lam, Yulin

supporting information, p. 704 - 712 (2020/11/30)

Indolecarboxamides are potent but poorly soluble mycobactericidal agents. Here we found that modifying the incipient scaffold by amide-amine substitution and replacing the indole ring with benzothiophene or benzoselenophene led to striking (10-20-fold) im

METHOD FOR PROMOTING PLANT GROWTH

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Page/Page column 22-23, (2012/12/13)

Disclosed is a method for promoting the growth of a plant, comprising treating the plant with an effective amount of a compound represented by the following formula (1):, wherein any one of R1, R2, R3 and R4 represents a trifluoromethyl group, and the others represent a hydrogen atom, or an agriculturally acceptable salt thereof.

TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF KINASES

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Page/Page column 84, (2010/11/27)

The present invention provides inhibitors of kinases, specifically IκB kinases, JAKl , JAK2, JAK3 and TYK2. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting said kinase activity by administering t

CHEMICAL COMPOUNDS

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Page/Page column 18, (2010/02/13)

A compound of formula (I) and pharmaceutically acceptable salts and solvates and hydrolysable esters thereof.

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