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279250-91-8

1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 279250-91-8 Structure

  • Basic information

    1. Product Name: 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI)
    2. Synonyms: 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI)
    3. CAS NO:279250-91-8
    4. Molecular Formula: C9H6N4
    5. Molecular Weight: 170.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 279250-91-8.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI)(279250-91-8)
    11. EPA Substance Registry System: 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI)(279250-91-8)

  • 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: 279250-91-8(Hazardous Substances Data)

279250-91-8 Usage

General Description

1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI) is a chemical compound with a molecular formula C9H6N4. It is a derivative of imidazole and pyridine. This chemical is commonly used in the pharmaceutical industry and has a wide range of applications. It has been studied for its potential use in the treatment of various medical conditions, including cancer, diabetes, and infectious diseases. Additionally, it is also used as a building block in the synthesis of various compounds and materials. Overall, 1H-Imidazole-4-carbonitrile, 2-(2-pyridinyl)- (9CI) is a versatile compound with diverse uses in the scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 279250-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,2,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 279250-91:
(8*2)+(7*7)+(6*9)+(5*2)+(4*5)+(3*0)+(2*9)+(1*1)=168
168 % 10 = 8
So 279250-91-8 is a valid CAS Registry Number.

279250-91-8SDS

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 2-(pyridin-2-yl)-1H-imidazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-(2-pyridyl)-4-cyano-1H-imidazole

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:279250-91-8 SDS

279250-91-8Relevant articles and documents

THERAPEUTIC COMPOUNDS AND USES THEREOF

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Paragraph 0353; 0354, (2015/03/16)

The present invention relates to compounds formula (I): and to salts thereof, wherein R1-R4 and A have any of the values defined in the specification, and compositions and uses thereof. The compounds are useful as inhibitors of histone demethylases, such as KDM5. Also included are pharmaceutically acceptable compositions comprising the compounds of the present invention and methods of using said compositions in the treatment of various disorders.

Synthesis, structure, and neuroprotective properties of novel imidazolyl nitrones

Dhainaut, Alain,Tizot, André,Raimbaud, Eric,Lockhart, Brian,Lestage, Pierre,Goldstein, Solo

, p. 2165 - 2175 (2007/10/03)

A new series of imidazolyl nitrones spin traps has been synthesized and evaluated pharmacologically. The salient structural feature of these molecules is the presence of an imidazole moiety substituted by aromatic or heteroaromatic cycles. This connectivi

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