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52532-63-5

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52532-63-5 Usage

Description

5-Aminothiophene-2-carbonitrile is a heterocyclic chemical compound with the molecular formula C5H4N2S. It features a thiophene ring with an amino group and a nitrile group attached to it, making it a versatile building block in organic synthesis. Its unique structure contributes to its value in the development of diverse chemical compounds for various industrial and scientific applications.

Uses

Used in Pharmaceutical Synthesis:
5-Aminothiophene-2-carbonitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 5-Aminothiophene-2-carbonitrile is used as a key component in the creation of various agrochemicals, aiding in the development of products designed to enhance crop protection and yield.
Used in Material Science:
5-Aminothiophene-2-carbonitrile is utilized as a building block in material science for its potential to contribute to the development of new materials with unique properties, such as in the creation of organic electronic devices or advanced polymers.
Used in Organic Synthesis:
As a versatile component in organic synthesis, 5-Aminothiophene-2-carbonitrile is used for the synthesis of a wide range of chemical compounds, including those with potential applications in various industries.
Used in Biological Activity Research:
5-Aminothiophene-2-carbonitrile is studied for its potential biological activities, such as antimicrobial and antiviral properties, making it a candidate for use in the development of treatments and preventive measures against infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 52532-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52532-63:
(7*5)+(6*2)+(5*5)+(4*3)+(3*2)+(2*6)+(1*3)=105
105 % 10 = 5
So 52532-63-5 is a valid CAS Registry Number.

52532-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminothiophene-2-carbonitrile

1.2 Other means of identification

Product number -
Other names GISCGLDZXOXKBZ-UHFFFAOYSA

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:52532-63-5 SDS

52532-63-5Downstream Products

52532-63-5Relevant articles and documents

MODIFIED PROTEINS AND PROTEIN DEGRADERS

-

Paragraph 00963-00965, (2021/12/08)

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

METHOD FOR THE PREPARATION OF FUSED HETEROCYCLIC SUCCINIMIDE COMPOUNDS AND ANALOGS THEREOF

-

, (2008/06/13)

Fused cyclic compounds, methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders, and pharmaceutical compositions containing such compounds.

2-Aminothiabutadiene as useful building block in the synthesis of 2-aminothiopyrans and 2-aminothiophenes

Robin, Aelig,Meslin, Jean-Claude,Deniaud, David

, p. 1633 - 1640 (2007/10/03)

We report a reliable and regiocontrolled alternative route to unsubstituted 2-aminothiopyrans and 2-aminothiophenes. These sulfur heterocycles were prepared by reaction of protected aminothiabutadiene 1 with acrylic dienophiles or acceptor-substituted halomethyl compounds. All compounds were fully characterized by IR, HRMS, and 13C and 1H NMR spectroscopy.

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