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132317-05-6

(1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132317-05-6 Structure

  • Basic information

    1. Product Name: (1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine
    2. Synonyms: (1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine
    3. CAS NO:132317-05-6
    4. Molecular Formula:
    5. Molecular Weight: 422.524
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132317-05-6.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: (1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine(132317-05-6)
    11. EPA Substance Registry System: (1S,6S,8aS)-octahydro-1-acetoxy-6-indolizine(132317-05-6)

  • 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: 132317-05-6(Hazardous Substances Data)

132317-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132317-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132317-05:
(8*1)+(7*3)+(6*2)+(5*3)+(4*1)+(3*7)+(2*0)+(1*5)=86
86 % 10 = 6
So 132317-05-6 is a valid CAS Registry Number.

132317-05-6Relevant articles and documents

Synthesis of (-)-Slaframine and Related Indolizidines

Pearson, William H.,Bergmeier, Stephen C.,Williams, John P.

, p. 3977 - 3987 (2007/10/02)

An enantioselective synthesis of the indolizidine alkaloid (-)-slaframine 1 is reported.Reductive double cyclization of the azido epoxy tosylate 48 afforded the indolizidine 52, which was converted to (-)-slaframine in two steps.The cyclization substrate

A Synthesis of (-)-Slaframine and (-)-1,8a-Diepislaframine

Pearson, William H.,Bergmeier, Stephen C.

, p. 1976 - 1978 (2007/10/02)

Reductive cyclization of the optically pure azido epoxides 12 and 13 afforded the indolizidines 14 and 16, which were converted into (-)-slaframine 1 and (-)-1,8a-diepislaframine 18.

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