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(1alpha,2beta,5alpha)-5-(isopropyl)-2-methylcyclohexyl acetate is a complex organic compound characterized by a cyclohexyl ring with multiple substituents, including an isopropyl and a methyl group. The presence of the acetate functional group indicates its derivation from acetic acid. The specific stereochemistry (1alpha,2beta,5alpha) denotes the spatial arrangement of the atoms in the molecule, which can influence its biological activity and interactions with other compounds. This chemical's unique properties and potential applications are shaped by its molecular structure and require further analysis and experimentation for a comprehensive understanding.

5256-66-6

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5256-66-6 Usage

Uses

Used in Pharmaceutical Industry:
(1alpha,2beta,5alpha)-5-(isopropyl)-2-methylcyclohexyl acetate is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique molecular structure and stereochemistry may contribute to the development of new therapeutic agents with specific biological activities.
Used in Flavor and Fragrance Industry:
Due to its complex molecular structure, (1alpha,2beta,5alpha)-5-(isopropyl)-2-methylcyclohexyl acetate is used as a component in the creation of unique fragrances and flavors. Its distinct properties can contribute to the development of novel scents and tastes in various consumer products.
Used in Chemical Research:
(1alpha,2beta,5alpha)-5-(isopropyl)-2-methylcyclohexyl acetate serves as a valuable compound for chemical research, particularly in the study of stereochemistry, molecular interactions, and the development of new synthetic methods. Its unique structure and properties make it an interesting subject for scientific investigation.
Used in Material Science:
(1alpha,2beta,5alpha)-5-(isopropyl)-2-methylcyclohexyl acetate's molecular structure and properties may also find applications in material science, where it could be utilized in the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5256-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5256-66:
(6*5)+(5*2)+(4*5)+(3*6)+(2*6)+(1*6)=96
96 % 10 = 6
So 5256-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h8-9,11-12H,5-7H2,1-4H3/t9-,11-,12-/m0/s1

5256-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-(R)-menthyl 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:5256-66-6 SDS

5256-66-6Upstream product

5256-66-6Downstream Products

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