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CAS

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157948-98-6

N-Allyl-N-benzyl-N-(pent-3-ynyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157948-98-6 Structure

  • Basic information

    1. Product Name: N-Allyl-N-benzyl-N-(pent-3-ynyl)amine
    2. Synonyms: N-Allyl-N-benzyl-N-(pent-3-ynyl)amine
    3. CAS NO:157948-98-6
    4. Molecular Formula:
    5. Molecular Weight: 213.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157948-98-6.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: N-Allyl-N-benzyl-N-(pent-3-ynyl)amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Allyl-N-benzyl-N-(pent-3-ynyl)amine(157948-98-6)
    11. EPA Substance Registry System: N-Allyl-N-benzyl-N-(pent-3-ynyl)amine(157948-98-6)

  • 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: 157948-98-6(Hazardous Substances Data)

157948-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157948-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,9,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 157948-98:
(8*1)+(7*5)+(6*7)+(5*9)+(4*4)+(3*8)+(2*9)+(1*8)=196
196 % 10 = 6
So 157948-98-6 is a valid CAS Registry Number.

157948-98-6Downstream Products

157948-98-6Relevant articles and documents

Zirconocene-mediated synthesis of 3,4-disubstituted piperidines and reduced isoquinolines

Kemp, Mark I.,Whitby, Richard J.,Coote, Steven J.

, p. 557 - 568 (2007/10/03)

Intramolecular cocyclisation of 4-azaocta-1,7-dienes, -1-en-7-ynes, -7- en-1-ynes and -1,7-diynes using 'zirconocene' equivalents affords 3-aza-8- zirconabicyclo[4.3.0]nonanes, -6-enes, -9-enes or -6,9-dienes. Protonolysis, iodinolysis, or carbonylation of these complexes affords 3,4-disubstitued piperidines. Exocyclic 1,3-dienes formed from the coupling/protonolysis of 4- azaocta-1,7-diynes react with activated dienophiles to yield reduced isoquinolines.

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