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2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 360566-07-0 Structure
  • Basic information

    1. Product Name: 2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester
    2. Synonyms: 2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester
    3. CAS NO:360566-07-0
    4. Molecular Formula:
    5. Molecular Weight: 329.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 360566-07-0.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: 2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester(360566-07-0)
    11. EPA Substance Registry System: 2-((E)-4-Oxo-oct-2-enyl)-pyrrolidine-1-carboxylic acid benzyl ester(360566-07-0)
  • 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: 360566-07-0(Hazardous Substances Data)

360566-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360566-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,5,6 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 360566-07:
(8*3)+(7*6)+(6*0)+(5*5)+(4*6)+(3*6)+(2*0)+(1*7)=140
140 % 10 = 0
So 360566-07-0 is a valid CAS Registry Number.

360566-07-0Downstream Products

360566-07-0Relevant articles and documents

A convenient allylsilane-N-acyliminium route toward 5-alkylindolizidines. Diastereoselective synthesis of (±)-indolizidine 167B

Peroche, Sandrine,Remuson, Roland,Gelas-Mialhe, Yvonne,Gramain, Jean-Claude

, p. 4617 - 4619 (2007/10/03)

A highly diastereoselective synthesis of 5-alkylindolizidines is described via an intermolecular addition of the allylsilyl functional group of homoallylic alcohols with an N-acyliminium ion derived from pyrrolidin-2-one.

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