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CAS

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279251-08-0

1H-Imidazole-4-carboxaldehyde, 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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  • 279251-08-0 Structure

  • Basic information

    1. Product Name: 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)- (9CI)
    2. Synonyms: 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)- (9CI)
    3. CAS NO:279251-08-0
    4. Molecular Formula: C9H7N3O
    5. Molecular Weight: 173.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 279251-08-0.mol

  • Chemical Properties

    1. Melting Point: 170 °C
    2. Boiling Point: 462.2±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.320±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.15±0.10(Predicted)
    10. CAS DataBase Reference: 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)- (9CI)(279251-08-0)
    12. EPA Substance Registry System: 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)- (9CI)(279251-08-0)

  • 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: 279251-08-0(Hazardous Substances Data)

279251-08-0 Usage

Heterocyclic compound

Containing both imidazole and pyridine rings The compound has a complex structure with two different heterocyclic rings, which are rings containing more than one type of atom, in this case, carbon and nitrogen.

Reactivity

Often used as a building block for the synthesis of various pharmaceuticals and organic compounds Due to its chemical properties, this compound readily reacts with other substances, making it a valuable component in creating new pharmaceuticals and organic compounds.

Versatile nature

Capable of参与 various chemical reactions The compound's versatile structure allows it to engage in numerous chemical reactions, such as oxidation and reduction processes.

Research reagent

Used in the field of organic chemistry and medicinal chemistry As a result of its unique properties and reactivity, 1H-Imidazole-4-carboxaldehyde, 2-(2-pyridinyl)-(9CI) is commonly used as a research reagent to help scientists develop new and novel synthetic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 279251-08-0 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 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 279251-08:
(8*2)+(7*7)+(6*9)+(5*2)+(4*5)+(3*1)+(2*0)+(1*8)=160
160 % 10 = 0
So 279251-08-0 is a valid CAS Registry Number.

279251-08-0SDS

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-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-Imidazole-5-carboxaldehyde,2-(2-pyridinyl)

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:279251-08-0 SDS

279251-08-0Downstream Products

279251-08-0Relevant articles and documents

NEW ANTIBACTERIAL COMPOUNDS

-

Page/Page column 53; 54, (2018/01/19)

The present invention relates to novel antibacterial compounds, pharmaceutical compositions containing them and their use as antimicrobials.

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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