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7785-54-8

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7785-54-8 Usage

Description

(R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is a cyclohexene derivative and an alkyl acetate, characterized by its cyclohexene ring structure with four methyl groups and a methyl acetate side chain. This chemical compound is known for its pleasant, fruity odor and is often used in various industries for its fragrance properties.

Uses

Used in Fragrance Industry:
(R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is used as a fragrance ingredient for its pleasant, fruity odor. It is commonly added to perfumes and other scented products to enhance their aroma.
Used in Cosmetics and Personal Care Industry:
(R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is used as a component in the manufacturing of cosmetics, soaps, and other personal care products, where its fragrance properties contribute to the overall sensory experience of these products.
Used in Pharmaceutical Industry:
(R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is utilized in the synthesis of pharmaceuticals, where its unique chemical structure may contribute to the development of new medications.
Used in Food Industry:
(R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate is used as a flavoring agent in the food industry, adding a fruity taste to various food products.
Safety Measures:
It is important to use (R)-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate with caution and follow proper safety measures due to its potential hazards if not handled correctly.

Check Digit Verification of cas no

The CAS Registry Mumber 7785-54-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7785-54:
(6*7)+(5*7)+(4*8)+(3*5)+(2*5)+(1*4)=138
138 % 10 = 8
So 7785-54-8 is a valid CAS Registry Number.

7785-54-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-(-)-α-terpinyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7785-54-8 SDS

7785-54-8Relevant 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.

Solvomercuration-Demercuration of Limonene with Hg(BF4)2; A Chemo- and Regiospecific Route to 8-Substituted p-Menthenes

Mattos, Marcio C.S. de,Kover, W. Bruce,Aznar, Fernando,Barluenga, Jose

, p. 4863 - 4866 (2007/10/02)

Solvomercuration-demercuration of limonene with equimolar Hg(BF4)2 and excess nucleophile (-20 deg C) functionalizes the acyclic double bond and provides specifically 8-substituted p-menthenes.Key words: limonene; mercuration-demercuration; α-terpineol; mercuric tetrafluoroborate; p-menthenes

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