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120167-83-1

7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120167-83-1 Structure

  • Basic information

    1. Product Name: 7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester
    2. Synonyms: 7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester
    3. CAS NO:120167-83-1
    4. Molecular Formula:
    5. Molecular Weight: 453.75
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120167-83-1.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: 7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester(120167-83-1)
    11. EPA Substance Registry System: 7-(Acetyl-octadecyl-amino)-heptanoic acid methyl ester(120167-83-1)

  • 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: 120167-83-1(Hazardous Substances Data)

120167-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120167-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,6 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120167-83:
(8*1)+(7*2)+(6*0)+(5*1)+(4*6)+(3*7)+(2*8)+(1*3)=91
91 % 10 = 1
So 120167-83-1 is a valid CAS Registry Number.

120167-83-1Downstream Products

120167-83-1Relevant articles and documents

Syntheses d'amidoesters par reaction de Kolbe

Abderrahman, Ben Moufida,Laurent, Eliane,Marquet, Bernard

, p. 571 - 578 (2007/10/02)

The synthesis of amidoesters has been investigated by anodic cooxidation of diacid hemiesters CO2H-CH2-Z-CO2CH3 -CH2-> and amidoacids R1-N(Y)-(CH2)2-CO2H .The scope of this reaction was examined in detail.This synthetic pathway provided very a simple access to a wide range of amidoesters R1-N(Y)-(CH2)3-Z-CO2CH3 by varying Z and R1 as well as n value.

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