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CAS

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143771-09-9

1-Pyrrolidinecarboxylic acid, 2-(4-oxoheptyl)-, phenylmethyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143771-09-9 Structure

  • Basic information

    1. Product Name: 1-Pyrrolidinecarboxylic acid, 2-(4-oxoheptyl)-, phenylmethyl ester, (R)-
    2. Synonyms:
    3. CAS NO:143771-09-9
    4. Molecular Formula: C19H27NO3
    5. Molecular Weight: 317.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143771-09-9.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-Pyrrolidinecarboxylic acid, 2-(4-oxoheptyl)-, phenylmethyl ester, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-(4-oxoheptyl)-, phenylmethyl ester, (R)-(143771-09-9)
    11. EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-(4-oxoheptyl)-, phenylmethyl ester, (R)-(143771-09-9)

  • 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: 143771-09-9(Hazardous Substances Data)

143771-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143771-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,7 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143771-09:
(8*1)+(7*4)+(6*3)+(5*7)+(4*7)+(3*1)+(2*0)+(1*9)=129
129 % 10 = 9
So 143771-09-9 is a valid CAS Registry Number.

143771-09-9Downstream Products

143771-09-9Relevant articles and documents

Expedient syntheses of indolizidines (-)-167B and (-)-209D

Kim, Guncheol,Lee, Eun-ju

, p. 2073 - 2076 (2007/10/03)

Indolizidine alkaloids (-)-167B and (-)-209D were synthesized via an expedient route using hydroacylation and amination.

Enantioselective Synthesis of (5R,9R)-5-Propyl-octahydroindolizine

Fleurant, Anne,Celerier, Jean Pierre,Lhommet, Gerard

, p. 695 - 696 (2007/10/02)

A versatile and practical synthesis of the dendrobatid alkaloid 167B is described using a chiral amino acid as starting material.

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