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CAS

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89814-99-3

1-(benzylideneamino)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89814-99-3 Structure

  • Basic information

    1. Product Name: 1-(benzylideneamino)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
    2. Synonyms:
    3. CAS NO:89814-99-3
    4. Molecular Formula: C15H13N3O
    5. Molecular Weight: 251.2832
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89814-99-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 387.1°C at 760 mmHg
    3. Flash Point: 187.9°C
    4. Appearance: N/A
    5. Density: 1.11g/cm3
    6. Vapor Pressure: 3.37E-06mmHg at 25°C
    7. Refractive Index: 1.59
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(benzylideneamino)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(benzylideneamino)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile(89814-99-3)
    12. EPA Substance Registry System: 1-(benzylideneamino)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile(89814-99-3)

  • 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: 89814-99-3(Hazardous Substances Data)

89814-99-3 Usage

Chemical class

Dihydropyridine derivative

Molecular structure

Contains a benzylideneamino group and a carbonitrile group

Pharmacological properties

Potential for use in medicinal chemistry for the development of new drugs

Applications

Organic synthesis, chemical processes, and further research in chemistry and pharmaceuticals

Reactivity

The presence of the benzylideneamino and carbonitrile groups suggests interesting reactivity

Biological activity

Potential for exhibiting biological activity due to its unique molecular structure

Research potential

A target for further research and exploration in the field of chemistry and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 89814-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89814-99:
(7*8)+(6*9)+(5*8)+(4*1)+(3*4)+(2*9)+(1*9)=193
193 % 10 = 3
So 89814-99-3 is a valid CAS Registry Number.

89814-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzylideneamino)-4,6-dimethyl-2-oxopyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:89814-99-3 SDS

89814-99-3Downstream Products

89814-99-3Relevant articles and documents

Pyrolysis of amino nitriles, cyanohydrazones, and cyanoacetamides. Part I. Elimination reaction of 1-arylmethyleneamino-1,2-dihydro-4, 6-dimethyl-2-oxopyridine-3-carbonitriles and substituted benzaldehyde cyanoacetylhydrazones

Al-Awadi,Elnagdi,Mathew,El-Gamry,Abdel Khalik

, p. 741 - 748 (2007/10/03)

Pyrolysis of the Schiff bases of 1-arylmethyleneamino-1,2-dihydro-4, 6-dimethyl-2-oxopyridine-3-carbonitriles (1-5) has been studied. These compounds eliminate via a six-membered transition state to produce substituted benzonitriles and 2-hydroxy-4,6-dimethylpyridine-3-carbonitrile. These eliminations are unimolecular first-order reactions. The kinetic data gave a good correlation with σ0 values of the substituents on the aryl group with ρ = 0.83 at 520 K. Utilization of the pyrolytic reaction in synthesis of various benzonitriles is considered, and mechanistic information has been obtained by comparing the kinetic data and product analysis of the Schiff bases with their open-chain substituted benzaldehyde cyanoacetylhydrazones (6-9) analogues.

Nitriles in Heterocyclic Synthesis: New Approaches for Synthesis of Some Pyridine Derivatives

Ibrahim, N. S.,Mohareb, R. M.,Shams, H. Z.

, p. 1351 - 1354 (2007/10/02)

A variety of pyridines was prepared from reaction of N-benzylidenecyanoethanoic hydrazide (2) with malononitrile, benzoylacetonitrile, cyanoacetamide and cinnamonitrile derivatives.The reactivity of 2 towards a variety of ketones was studied. - Keywords:

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