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121952-67-8

5-Hydroxy-5-(4-methyl-cyclohex-3-enyl)-hexanoic 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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  • 121952-67-8 Structure

  • Basic information

    1. Product Name: 5-Hydroxy-5-(4-methyl-cyclohex-3-enyl)-hexanoic acid methyl ester
    2. Synonyms:
    3. CAS NO:121952-67-8
    4. Molecular Formula:
    5. Molecular Weight: 240.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121952-67-8.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: 5-Hydroxy-5-(4-methyl-cyclohex-3-enyl)-hexanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Hydroxy-5-(4-methyl-cyclohex-3-enyl)-hexanoic acid methyl ester(121952-67-8)
    11. EPA Substance Registry System: 5-Hydroxy-5-(4-methyl-cyclohex-3-enyl)-hexanoic acid methyl ester(121952-67-8)

  • 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: 121952-67-8(Hazardous Substances Data)

121952-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121952-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,5 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121952-67:
(8*1)+(7*2)+(6*1)+(5*9)+(4*5)+(3*2)+(2*6)+(1*7)=118
118 % 10 = 8
So 121952-67-8 is a valid CAS Registry Number.

121952-67-8Relevant articles and documents

SYNTHESIS OF BISABOL-10-ENE-3,7-OXIDE

Pascual-T., J. de,Hernandez, M. L.,Moran, J. R.,Caballero, C.,Anaya, J.,Alcazar, V.

, p. 5109 - 5112 (2007/10/02)

The synthesis of bisabol-10-ene-3,7-oxide was accomplished using as the key intermediate a radical obtained in the reduction of an organomercuric compound, and starting either from limonene or β-terpineol.

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