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2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID is a chemical compound with the molecular formula C9H10O2S, belonging to the thiophene family. It features a carboxylic acid functional group and two methyl substituents on the thiophene ring, which contribute to its unique chemical properties and potential applications in various fields.

26421-32-9

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26421-32-9 Usage

Uses

Used in Organic Synthesis:
2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID is used as a building block and intermediate in organic synthesis for the development of various biologically active molecules. Its unique structure allows for the creation of diverse chemical compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID is utilized as a key intermediate for the synthesis of new drugs. Its ability to modulate biological pathways and target specific protein binding sites makes it a promising candidate for the development of innovative therapeutic agents.
Used in Agrochemical Development:
2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID also shows potential in the agrochemical sector, where it can be used as a building block for the synthesis of new agrochemicals. Its unique properties may contribute to the development of more effective and targeted pesticides or other agricultural products.
Used in Advanced Materials Development:
In the field of materials science, 2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID has been investigated for its potential use in the development of advanced materials. Its unique chemical properties may contribute to the creation of new materials with improved performance characteristics.
Used in Coordination Chemistry:
2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID has also shown potential as a ligand in coordination chemistry. Its ability to form stable complexes with various metal ions can be utilized in the development of new catalysts, sensors, or other functional materials with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 26421-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26421-32:
(7*2)+(6*6)+(5*4)+(4*2)+(3*1)+(2*3)+(1*2)=89
89 % 10 = 9
So 26421-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2S/c1-4-3-6(7(8)9)5(2)10-4/h3H,1-2H3,(H,8,9)

26421-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-DIMETHYLTHIOPHENE-3-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 2,5-dimethyl-3-thiophenecarboxylic 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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26421-32-9 SDS

26421-32-9Relevant academic research and scientific papers

SULFONYLUREA DERIVATIVES AND USES THEREOF

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Paragraph 0951-0952, (2020/12/30)

The present disclosure relates to compounds of Formula (I) and to their prodrugs, pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds disclosed herein are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes and may be used in the treatment of disorders in which inflammasome activity is implicated, such as inflammatory, autoinflammatory and autoimmune diseases and cancers.

Synthesis and photochromic properties of tetrakis(3,5-dimethyl-2-thienyl)- and tetrakis(2,5-dimethyl-3-thienyl)ethylenes

Belen'kii,Gromova,Kolotaev,Nabatov,Krayushkin

, p. 1208 - 1213 (2007/10/03)

Tetrakis(3,5-dimethyl-2-thienyl)ethylene and tetrakis(2,5-dimethyl-3- thienyl)ethylene were obtained from the corresponding dithienyl ketones by the McMurry reaction. The photochromic properties of the compounds obtained were studied.

Phosphorylamides, their preparation and use

-

, (2008/06/13)

A phosphorylamide derivative represented by the general formula (I): STR1 wherein R represents an amino group that may be substituted, or a salt thereof, possesses potent antibacterial activity against Helicobacter bacterium, especially Helicobacter pylori, and is useful for prevention or treatment of digestive diseases caused by Helicobacter bacterium, solely or in combination with an antacid or an acid secretion inhibitor.

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