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122020-56-8

4-Butyl-N-((Z)-octadec-9-enyl)-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122020-56-8 Structure

  • Basic information

    1. Product Name: 4-Butyl-N-((Z)-octadec-9-enyl)-benzamide
    2. Synonyms:
    3. CAS NO:122020-56-8
    4. Molecular Formula:
    5. Molecular Weight: 427.714
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122020-56-8.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: 4-Butyl-N-((Z)-octadec-9-enyl)-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Butyl-N-((Z)-octadec-9-enyl)-benzamide(122020-56-8)
    11. EPA Substance Registry System: 4-Butyl-N-((Z)-octadec-9-enyl)-benzamide(122020-56-8)

  • 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: 122020-56-8(Hazardous Substances Data)

122020-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122020-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122020-56:
(8*1)+(7*2)+(6*2)+(5*0)+(4*2)+(3*0)+(2*5)+(1*6)=58
58 % 10 = 8
So 122020-56-8 is a valid CAS Registry Number.

122020-56-8Relevant articles and documents

Potential Antiatherosclerotic Agents. 6. Hypocholesterolemic Trisubstituted Urea Analogues

DeVries, Vern G.,Bloom, Jonathan D.,Dutia, Minu D.,Katocs, Andrew S.,Largis, Elwood E.

, p. 2318 - 2325 (2007/10/02)

The discovery that a series of N,N-dialkyl-N'-arylureas were inhibitors of the ACAT enzyme has led to a structure-activity study involving the systematic modification of three sites of the urea backbone.This study culminated in the selection of N'-(2,4-dimethylphenyl)-N-benzyl-N-n-butylurea (115) for more extensive biological evaluation.ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.

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