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232280-77-2

4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE is a heterocyclic aromatic compound with the molecular formula C6H5N3S. It features a thiophene ring with an aminomethyl group and a cyano group attached at the 2nd and 4th positions, respectively. This versatile chemical compound is widely used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential biological and pharmacological activities, including anti-cancer and anti-inflammatory properties.

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  • 232280-77-2 Structure

  • Basic information

    1. Product Name: 4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE
    2. Synonyms: 4-(aminomethyl)-2-thiophenecarbonitrile
    3. CAS NO:232280-77-2
    4. Molecular Formula: C6H6N2S
    5. Molecular Weight: 138.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 232280-77-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE(232280-77-2)
    11. EPA Substance Registry System: 4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE(232280-77-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 232280-77-2(Hazardous Substances Data)

232280-77-2 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE is used as a building block for the synthesis of various pharmaceuticals due to its versatile nature and potential biological and pharmacological activities.
Used in Agrochemical Industry:
4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE is used as a building block for the synthesis of various agrochemicals, contributing to the development of new and effective products in this field.
Used in Organic Synthesis:
4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE is used as a valuable intermediate in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications.
Used in Biological and Pharmacological Research:
4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE is used in research for its potential anti-cancer and anti-inflammatory properties, offering new avenues for the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 232280-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,2,8 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 232280-77:
(8*2)+(7*3)+(6*2)+(5*2)+(4*8)+(3*0)+(2*7)+(1*7)=112
112 % 10 = 2
So 232280-77-2 is a valid CAS Registry Number.

232280-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(aminomethyl)thiophene-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-AMINOMETHYL-THIOPHENE-2-CARBONITRILE

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:232280-77-2 SDS

232280-77-2Relevant articles and documents

Noncovalent tripeptidic thrombin inhibitors incorporating amidrazone, amine and amidine functions at P1

Lee, Koo,Jung, Won-Hyuk,Park, Cheol Won,Park, Hee Dong,Lee, Sun Hwa,Kwon, O Hwan

, p. 1017 - 1022 (2007/10/03)

A series of noncovalent tripeptidic thrombin inhibitors incorporating amidrazone, amine and amidine functions at P1 was investigated. While the amidrazone and the amine series displayed limited oral absorption, the amidine series demonstrated generally good oral absorption and strong antithrombotic activity; the single-digit picomolar Ki achieved from this series is among the best yet reported. The present work highlights the benzamidine compound 11f (LB30812) that exhibits excellent overall profiles of potency, oral absorption and antithrombotic efficacy.

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