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CAS

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121401-07-8

(4S,5S)-2-Hydroxy-5-isopropenyl-4-methyl-4-vinyl-cyclohex-1-enecarboxylic 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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  • 121401-07-8 Structure

  • Basic information

    1. Product Name: (4S,5S)-2-Hydroxy-5-isopropenyl-4-methyl-4-vinyl-cyclohex-1-enecarboxylic acid methyl ester
    2. Synonyms:
    3. CAS NO:121401-07-8
    4. Molecular Formula:
    5. Molecular Weight: 236.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121401-07-8.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: (4S,5S)-2-Hydroxy-5-isopropenyl-4-methyl-4-vinyl-cyclohex-1-enecarboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-2-Hydroxy-5-isopropenyl-4-methyl-4-vinyl-cyclohex-1-enecarboxylic acid methyl ester(121401-07-8)
    11. EPA Substance Registry System: (4S,5S)-2-Hydroxy-5-isopropenyl-4-methyl-4-vinyl-cyclohex-1-enecarboxylic acid methyl ester(121401-07-8)

  • 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: 121401-07-8(Hazardous Substances Data)

121401-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121401-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121401-07:
(8*1)+(7*2)+(6*1)+(5*4)+(4*0)+(3*1)+(2*0)+(1*7)=58
58 % 10 = 8
So 121401-07-8 is a valid CAS Registry Number.

121401-07-8Relevant articles and documents

TOTAL SYNTHESIS OF VARIOUS ELEMANOLIDES

Friedrich, Dirk,Bohlmann, Ferdinand

, p. 1369 - 1392 (1988)

Starting with a suitable substituted divinyl cyclohexanone, eleven naturally occurring 12.8-elemanolides bearing exo-methylene or methyl groups at C-11 and differing in substitution as well as in relative configuration, have been synthesized in racemic form.An approach to elemanolides with additional oxygen functionalities is principally possible by modification of the basic concept.Methods for the oxidative generation of terpenoid exo-methylene lactone and furan units are exemplified by synthesis of menthofuran and the p-menthenolides from isopulegols.

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