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3-Amino-4-methyl-2-thiophenecarboxylic acid is a heterocyclic chemical compound with the molecular formula C6H7NO2S. It features a carboxylic acid derivative with an amino group and a methyl substitution on a thiophene ring, contributing to its unique chemical properties and potential applications in various fields.

23968-18-5

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23968-18-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3-Amino-4-methyl-2-thiophenecarboxylic acid is used as a building block in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties, enhancing the effectiveness of drugs and pesticides.
Used in Organic Synthesis:
3-AMINO-4-METHYL-2-THIOPHENECARBOXYLIC ACID is utilized in organic synthesis as a versatile reagent, enabling the creation of a wide range of organic molecules. Its ability to participate in various chemical reactions, such as condensation, substitution, and addition, makes it a valuable component in the synthesis of complex organic compounds.
Used in Chemical Reactions as a Reagent:
3-Amino-4-methyl-2-thiophenecarboxylic acid serves as a reagent in chemical reactions, facilitating the formation of desired products. Its presence can influence the reaction pathway, yield, and selectivity, making it an essential component in various chemical processes.
Used in the Development of New Materials:
3-AMINO-4-METHYL-2-THIOPHENECARBOXYLIC ACID has potential applications in the development of new materials, such as polymers, dyes, and sensors, due to its unique chemical properties. Its ability to form stable complexes and participate in redox reactions can contribute to the creation of innovative materials with specific functionalities.
Used as a Research Tool in Organic Chemistry:
3-Amino-4-methyl-2-thiophenecarboxylic acid is employed as a research tool in the field of organic chemistry, aiding scientists in understanding reaction mechanisms, exploring new synthetic routes, and discovering novel compounds with potential applications. Its versatility and reactivity make it a valuable asset in advancing the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 23968-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,6 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23968-18:
(7*2)+(6*3)+(5*9)+(4*6)+(3*8)+(2*1)+(1*8)=135
135 % 10 = 5
So 23968-18-5 is a valid CAS Registry Number.

23968-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-methylthiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-amino 4-methylthiophene-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23968-18-5 SDS

23968-18-5Relevant academic research and scientific papers

Conformationally-restricted amino acid analogues bearing a distal sulfonic acid show selective inhibition of system xc- over the vesicular glutamate transporter

Etoga, Jean-Louis G.,Ahmed, S. Kaleem,Patel, Sarjubhai,Bridges, Richard J.,Thompson, Charles M.

scheme or table, p. 2680 - 2683 (2010/07/13)

A panel of amino acid analogs and conformationally-restricted amino acids bearing a sulfonic acid were synthesized and tested for their ability to preferentially inhibit the obligate cysteine-glutamate transporter system xc- versus t

2-AMINOPYRIDINE ANALOGS AS GLUCOKINASE ACTIVATORS

-

Page/Page column 58, (2008/12/04)

Provided are compounds that are useful in the treatment and/or prevention of diseases mediated by deficient levels of glucokinase activity, such as diabetes mellitus. Also provided are methods of treating or preventing diseases and disorders characterized by underactivity of glucokinase or which can be treated by activating glucokinase.

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