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1429649-64-8

C14H18BF2N2O(1+)*F(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429649-64-8 Structure

  • Basic information

    1. Product Name: C14H18BF2N2O(1+)*F(1-)
    2. Synonyms:
    3. CAS NO:1429649-64-8
    4. Molecular Formula:
    5. Molecular Weight: 298.116
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429649-64-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C14H18BF2N2O(1+)*F(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H18BF2N2O(1+)*F(1-)(1429649-64-8)
    11. EPA Substance Registry System: C14H18BF2N2O(1+)*F(1-)(1429649-64-8)

  • 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: 1429649-64-8(Hazardous Substances Data)

1429649-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429649-64-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,6,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1429649-64:
(9*1)+(8*4)+(7*2)+(6*9)+(5*6)+(4*4)+(3*9)+(2*6)+(1*4)=198
198 % 10 = 8
So 1429649-64-8 is a valid CAS Registry Number.

1429649-64-8Downstream Products

1429649-64-8Relevant articles and documents

Synthesis of 2-unsubstituted 1-arylimidazoles

Mityanov,Perevalov,Tkach

, p. 1793 - 1800 (2013)

A method has been developed for the synthesis of 1-arylimidazoles lacking a substituent at position 2, featuring the preparation of 1-arylimidazole N-oxides stabilized as boron trifluoride derivatives, with subsequent reduction to the desired imidazoles. This method permits broad variation of the substituents in the aryl part of these molecules.

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