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CAS

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157948-96-4

1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157948-96-4 Structure

  • Basic information

    1. Product Name: 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine
    2. Synonyms: 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine
    3. CAS NO:157948-96-4
    4. Molecular Formula:
    5. Molecular Weight: 295.468
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157948-96-4.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: 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine(157948-96-4)
    11. EPA Substance Registry System: 1-Benzyl-4-((E)-ethylidene)-3-((Z)-hept-6-enylidene)piperidine(157948-96-4)

  • 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: 157948-96-4(Hazardous Substances Data)

157948-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157948-96-4 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 157948-96:
(8*1)+(7*5)+(6*7)+(5*9)+(4*4)+(3*8)+(2*9)+(1*6)=194
194 % 10 = 4
So 157948-96-4 is a valid CAS Registry Number.

157948-96-4Downstream Products

157948-96-4Relevant 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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