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CYCLOHEXANEMETHANOL, 4-(1-METHYLETHYL)-, ACETATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

46337-76-2

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46337-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46337-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,3,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 46337-76:
(7*4)+(6*6)+(5*3)+(4*3)+(3*7)+(2*7)+(1*6)=132
132 % 10 = 2
So 46337-76-2 is a valid CAS Registry Number.

46337-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-propan-2-ylcyclohexyl)methyl acetate

1.2 Other means of identification

Product number -
Other names ACETIC ACID 4-ISOPROPYLCYCLOHEXYLMETHYL ESTER

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:46337-76-2 SDS

46337-76-2Downstream Products

46337-76-2Relevant academic research and scientific papers

Preparation and utilization of perillyl acetate

?tekrová, Martina,Paterová-Dudková, Iva,Vysko?ilová-Leitmannová, Eli?ka,?erveny, Libor

, p. 2075 - 2084 (2013/02/22)

Perillyl acetate is a fragrance compound that was prepared by the reaction of β-pinenoxide with acetic anhydride and using acetic acid as an acid catalyst. Several selected catalysts were tested (homogenous: phosphoric acid, boric acid, acetic acid, and citric acid; heterogeneous: zeolite USY, SSA, and montmorillonite K-10) and the reaction conditions optimized for this reaction. The yield 78.7 % of perillyl acetate was obtained. Mayol (4- isopropylcyclohexylmethanol), a valuable fragrance compound, was further obtained by a two-step synthesis from perillyl acetate. Firstly, perillyl acetate was saponified to perillyl alcohol. The yield of alcohol was 94.4 %. The last step of the entire preparation was the hydrogenation of perillyl alcohol to Mayol. The yield of the desired product of this reaction was 94.6 %. Springer Science+Business Media B.V. 2012.

Alicyclic compounds, their use and process for preparing same

-

, (2008/06/13)

Use of alicyclic compounds, some of which are new, as odor-modifying ingredients for manufacturing perfumes, perfumed products or synthetic essential oils, and as flavor-modifying ingredients for the manufacture of artificial flavors or for the aromatization of foodstuffs, animal feeds, pharmaceutical preparations or tobacco products. Process for preparing said alicyclic compounds.

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