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21486-28-2

3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE is a chemical compound belonging to the class of isoxazolecarbonitrile compounds. It is known for its diverse properties and activities, which include potential biological and pharmaceutical applications.
Used in Pharmaceutical Industry:
3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE is used as a potential bioactive molecule for its antimicrobial, antifungal, and herbicidal activities. Its unique chemical structure and properties make it a valuable candidate for further research and potential applications in the development of new drugs and therapies.
Used in Agricultural Industry:
3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE is used as a potential herbicide due to its herbicidal activities. Its effectiveness in controlling unwanted plant growth can contribute to more efficient and sustainable agricultural practices.
Used in Medical Research:
3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE is used as an enzyme inhibitor in the study of specific biological processes and diseases. Its potential as an inhibitor makes it a valuable tool for understanding the mechanisms of various conditions and for the development of targeted therapies.

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  • 21486-28-2 Structure

  • Basic information

    1. Product Name: 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE
    2. Synonyms: 3-(2,6-DICHLOROPHENYL)-5-METHYLISOXAZOLE-4-CARBONITRILE;3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE
    3. CAS NO:21486-28-2
    4. Molecular Formula: C11H6Cl2N2O
    5. Molecular Weight: 253.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21486-28-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 393°Cat760mmHg
    3. Flash Point: 191.5°C
    4. Appearance: /
    5. Density: 1.45g/cm3
    6. Vapor Pressure: 2.19E-06mmHg at 25°C
    7. Refractive Index: 1.615
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE(21486-28-2)
    12. EPA Substance Registry System: 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBONITRILE(21486-28-2)

  • 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: 21486-28-2(Hazardous Substances Data)

21486-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21486-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,8 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21486-28:
(7*2)+(6*1)+(5*4)+(4*8)+(3*6)+(2*2)+(1*8)=102
102 % 10 = 2
So 21486-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H6Cl2N2O/c1-6-7(5-14)11(15-16-6)10-8(12)3-2-4-9(10)13/h2-4H,1H3

21486-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,6-Dichlorophenyl)-5-methyl-1,2-oxazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-Cyano-3-(2,6-dichlorophenyl)-5-methylisoxazole

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:21486-28-2 SDS

21486-28-2Relevant articles and documents

Electrochemical and yeast-catalysed ring-opening of isoxazoles in the synthesis of analogues of the herbicide Grasp

Easton,Heath,Hughes,Lee,Savage,Simpson,Tiekink,Vuckovic,Webster

, p. 1168 - 1174 (2007/10/03)

Isoxazoles substituted with an electron-withdrawing group at the 4-position undergo electrochemical and yeast-catalysed N-O bond cleavage. The electrolysis is much more efficient and, with acyl- and alkoxycarbonyl-substituted isoxazoles, it affords the enolised dicarbonylimine functionality characteristic of the herbicide Grasp. Regioisomeric 4- and 5-substituted isoxazoles are accessible through nitrile oxide cycloaddition chemistry, using halogen as a steric auxiliary to control the regiochemistry of reaction. Crystal data for compounds 11 and 19b are presented.

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