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1073591-09-9

(S)-3,5,5-trimethyl-2-cyclohexen-1-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1073591-09-9 Structure

  • Basic information

    1. Product Name: (S)-3,5,5-trimethyl-2-cyclohexen-1-yl acetate
    2. Synonyms:
    3. CAS NO:1073591-09-9
    4. Molecular Formula:
    5. Molecular Weight: 182.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1073591-09-9.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: (S)-3,5,5-trimethyl-2-cyclohexen-1-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3,5,5-trimethyl-2-cyclohexen-1-yl acetate(1073591-09-9)
    11. EPA Substance Registry System: (S)-3,5,5-trimethyl-2-cyclohexen-1-yl acetate(1073591-09-9)

  • 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: 1073591-09-9(Hazardous Substances Data)

1073591-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073591-09-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,5,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1073591-09:
(9*1)+(8*0)+(7*7)+(6*3)+(5*5)+(4*9)+(3*1)+(2*0)+(1*9)=149
149 % 10 = 9
So 1073591-09-9 is a valid CAS Registry Number.

1073591-09-9Downstream Products

1073591-09-9Relevant articles and documents

Synthesis of chiral odoriferous oxy-derivatives of 1,5,5- trimethylcyclohexene

Winska,Wawrzenczyk

, p. 1887 - 1897 (2008/09/18)

Ten racemic and ten enantiomeric pairs of odoriferous compounds, mainly esters, were obtained from isophorone. The starting material, isophorone was reduced to racemic isophorol, which was resolved in pure enantiomers via the lipase catalyzed esterification. The next steps of syntheses, orthoacetic Claisen rearrangement, reduction of esters, esterification of alcohols or their oxidation were carried out with the racemic and enantiomerically enriched (above 98% ee) compounds. The propionates of isophorol (7, 7a, 7b) and 2-(1,5,5-trimethyl-2-cyclohexen-1-yl)ethanol (10, 10a, 10b) possess the most valuable odoriferous properties, useful for cosmetic and food industries.

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