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182343-62-0

1-Benzoyl-2-(prop-2-enyl)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182343-62-0 Structure

  • Basic information

    1. Product Name: 1-Benzoyl-2-(prop-2-enyl)piperidine
    2. Synonyms:
    3. CAS NO:182343-62-0
    4. Molecular Formula:
    5. Molecular Weight: 229.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182343-62-0.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-Benzoyl-2-(prop-2-enyl)piperidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Benzoyl-2-(prop-2-enyl)piperidine(182343-62-0)
    11. EPA Substance Registry System: 1-Benzoyl-2-(prop-2-enyl)piperidine(182343-62-0)

  • 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: 182343-62-0(Hazardous Substances Data)

182343-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182343-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,4 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 182343-62:
(8*1)+(7*8)+(6*2)+(5*3)+(4*4)+(3*3)+(2*6)+(1*2)=130
130 % 10 = 0
So 182343-62-0 is a valid CAS Registry Number.

182343-62-0Downstream Products

182343-62-0Relevant articles and documents

Synthesis of bridged azabicyclic compounds using radical translocation reactions of 1-(o-halogenobenzoyl)-2-(prop-2-enyl)-and -(prop-2-ynyl)-piperidines

Ikeda, Masazumi,Kugo, Yasuhiro,Sato, Tatsunori

, p. 1819 - 1824 (2007/10/03)

Methyl 1-(o-bromobenzoyl)-2-(prop-2-enyl)piperidine-2-carboxylate 8a, upon treatment with tributyltin hydride in the presence of azoisobutyronitrile in boiling toluene gave regioselectively the 8-azabicyclo[3.2.1]octane 14a (a 5-exo cyclisation product) in quantitative yield as a diastereomeric mixture (66:34). 1-(o-Bromobenzoyl)-2-(prop-2-enyl)piperidine 13 also gave the 8-azabicyclo-[3.2.1]octane 16 (75% as a diastereomeric mixture), along with the pyrido[2,1-a]isoindolone 17 (10%) and the simple reduction product 18 (5%). 1-(o-Iodobenzoyl)-2-[3-(trimethylsilyl)prop-2-ynyl]piperidine 23 afforded, in addition to the pyrido[2,1-a]isoindolone 25 (18%), the 8-azabicyclo-[3.2.1]octane 24 (75%) which was converted into the 6-oxo derivative 27. For comparison, the behaviour of the azetidine congener 31 was also examined.

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