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CAS

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86532-08-3

4-(4-Methyl-cyclohex-3-enyl)-pent-4-enenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86532-08-3 Structure

  • Basic information

    1. Product Name: 4-(4-Methyl-cyclohex-3-enyl)-pent-4-enenitrile
    2. Synonyms:
    3. CAS NO:86532-08-3
    4. Molecular Formula:
    5. Molecular Weight: 175.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86532-08-3.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-(4-Methyl-cyclohex-3-enyl)-pent-4-enenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-Methyl-cyclohex-3-enyl)-pent-4-enenitrile(86532-08-3)
    11. EPA Substance Registry System: 4-(4-Methyl-cyclohex-3-enyl)-pent-4-enenitrile(86532-08-3)

  • 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: 86532-08-3(Hazardous Substances Data)

86532-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86532-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,3 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86532-08:
(7*8)+(6*6)+(5*5)+(4*3)+(3*2)+(2*0)+(1*8)=143
143 % 10 = 3
So 86532-08-3 is a valid CAS Registry Number.

86532-08-3Downstream Products

86532-08-3Relevant articles and documents

SYNTHESIS OF NORBISABOLIDE

Ho, Tse-Lok

, p. 341 - 346 (2007/10/02)

Norbisabolide has been synthesized from limonen 8,9-oxide via malonate alkylation.In situ generation of the terpene synthon from 4-methyl-3-cyclohexen-1-yl methyl ketone is demonstrated.Homolimonenol can also serve as precursor of the terpene.

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