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62947-31-3

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62947-31-3 Usage

Description

Dimethyl 4-aminothiophene-2,3-dicarboxylate is a chemical compound characterized by the molecular formula C8H8N2O4S. It is a thiophene derivative featuring two carboxylate groups and a dimethylamino group at the 4-position of the thiophene ring. Dimethyl 4-aminothiophene-2,3-dicarboxylate is recognized for its potential applications in various fields, including pharmaceutical research and organic synthesis.

Uses

Used in Pharmaceutical Research:
Dimethyl 4-aminothiophene-2,3-dicarboxylate is utilized as a building block in the development of various drugs and biologically active molecules. Its unique structure and functional groups contribute to the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the realm of organic synthesis, Dimethyl 4-aminothiophene-2,3-dicarboxylate is employed as a key intermediate for the synthesis of complex organic compounds, leveraging its reactive carboxylate and dimethylamino groups.
Used in Anti-inflammatory and Analgesic Applications:
Dimethyl 4-aminothiophene-2,3-dicarboxylate is studied for its potential anti-inflammatory and analgesic properties, making it a candidate for the development of new medications aimed at treating pain and inflammation.
Used in Neurological Disorder Treatment:
Dimethyl 4-aminothiophene-2,3-dicarboxylate has been investigated for its potential use in the treatment of neurological disorders, suggesting that it may have neuroprotective or therapeutic effects on conditions affecting the nervous system.
Used in Fluorescent Dyes Synthesis:
Dimethyl 4-aminothiophene-2,3-dicarboxylate is also considered a precursor for the synthesis of fluorescent dyes, which are important in various applications such as bioimaging, diagnostics, and sensing.
Used in Organic Optoelectronic Materials:
Furthermore, it has been explored as a precursor for the synthesis of organic optoelectronic materials, which are crucial in the development of advanced electronic devices and technologies, including organic light-emitting diodes (OLEDs) and photovoltaic cells.

Check Digit Verification of cas no

The CAS Registry Mumber 62947-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,4 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62947-31:
(7*6)+(6*2)+(5*9)+(4*4)+(3*7)+(2*3)+(1*1)=143
143 % 10 = 3
So 62947-31-3 is a valid CAS Registry Number.

62947-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 4-Aminothiophene-2,3-Dicarboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl 4-aminothiophene-2,3-dicarboxylate

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:62947-31-3 SDS

62947-31-3Downstream Products

62947-31-3Relevant articles and documents

A rapid conversion of 3-oxothiolanes into 3-aminothiophenes

Barker, John M.,Huddleston, Patrick R.,Wood, Michael L.

, p. 2565 - 2568 (2007/10/03)

3-Oxotetrahydrothiophenes can be rapidly converted into 3-aminothiophenes by refluxing with hydroxylamine hydrochloride in a polar solvent, usually acetonitrile.

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