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1446146-99-1

C14H12(2)H6N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446146-99-1 Structure

  • Basic information

    1. Product Name: C14H12(2)H6N2O
    2. Synonyms: C14H12(2)H6N2O
    3. CAS NO:1446146-99-1
    4. Molecular Formula:
    5. Molecular Weight: 236.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446146-99-1.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: C14H12(2)H6N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H12(2)H6N2O(1446146-99-1)
    11. EPA Substance Registry System: C14H12(2)H6N2O(1446146-99-1)

  • 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: 1446146-99-1(Hazardous Substances Data)

1446146-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446146-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,1,4 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1446146-99:
(9*1)+(8*4)+(7*4)+(6*6)+(5*1)+(4*4)+(3*6)+(2*9)+(1*9)=171
171 % 10 = 1
So 1446146-99-1 is a valid CAS Registry Number.

1446146-99-1Downstream Products

1446146-99-1Relevant articles and documents

Synthesis of spirocyclic indolines by interruption of the Bischler-Napieralski reaction

Medley, Jonathan William,Movassaghi, Mohammad

supporting information, p. 3614 - 3617 (2013/08/23)

The development of a versatile method for the synthesis of spirocyclic pyrrolidinoindolines is discussed. Treatment of N-acyltryptamines with trifluoromethanesulfonic anhydride-2-chloropyridine reagent combination affords highly persistent spiroindoleninium ions that are subject to intra- and intermolecular addition at C2 by nucleophiles.

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