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(±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate is a complex chemical compound derived from cyclohexene, featuring a methyl acetate group. It is optically inactive, which means it does not rotate the plane of polarized light. (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate is known for its fruity odor, making it a valuable ingredient in various industries.

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  • 10581-37-0 Structure
  • Basic information

    1. Product Name: (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate
    2. Synonyms: (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate
    3. CAS NO:10581-37-0
    4. Molecular Formula:
    5. Molecular Weight: 196.29
    6. EINECS: 234-183-5
    7. Product Categories: N/A
    8. Mol File: 10581-37-0.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: (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate(10581-37-0)
    11. EPA Substance Registry System: (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate(10581-37-0)
  • 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: 10581-37-0(Hazardous Substances Data)

10581-37-0 Usage

Uses

Used in Food Industry:
(±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate is used as a flavoring agent for its fruity aroma, enhancing the taste and smell of various food products.
Used in Perfume and Fragrance Industry:
The pleasant smell of (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate makes it a suitable component in perfumes and fragrances, contributing to the overall scent profile of these products.
Used in Pharmaceutical Industry:
(±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate is utilized in the pharmaceutical industry, likely due to its unique chemical properties and potential applications in drug development or formulation.
Used in Cosmetic Industry:
(±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate also finds applications in the cosmetic industry, possibly for its scent or other properties that can contribute to the effectiveness or appeal of cosmetic products.
The stability of (±)-alpha,alpha,4-trimethylcyclohex-3-ene-1-methyl acetate under normal conditions allows for its safe handling and storage in dry, cool environments, making it a practical choice for use across these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 10581-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10581-37:
(7*1)+(6*0)+(5*5)+(4*8)+(3*1)+(2*3)+(1*7)=80
80 % 10 = 0
So 10581-37-0 is a valid CAS Registry Number.

10581-37-0Relevant articles and documents

Heteropoly acid catalysts for the synthesis of fragrance compounds from bio-renewables: Acetylation of nopol and terpenic alcohols

Costa, Vinicius V.,Da Silva Rocha, Kelly A.,Oliveira, Luiz C. A.,Kozhevnikova, Elena F.,Kozhevnikov, Ivan V.,Gusevskaya, Elena V.

, p. 43217 - 43222 (2016/05/24)

The cesium salt of tungstophosphoric heteropoly acid, Cs2.5H0.5PW12O40, is an active and environmentally friendly heterogeneous catalyst for the liquid-phase acetylation of nopol and several biomass-derived terpenic alcohols (i.e., α-terpineol, nerol, geraniol, linalool, menthol, isoborneol, perillyl alcohol, carveol, isopulegol, carvacrol and nerolidol) with acetic anhydride. The resulting flavor and fragrance acetic esters, which are widely used in perfumery, household and food products, are obtained in good to excellent yields. The reactions occur at room temperature with low catalyst loadings without substantial catalyst leaching and can be performed with stoichiometric amounts of an acetylating agent in solvent free systems.

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