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(3R,5R)-3,5-dimethylcyclohexanol is a colorless liquid chemical compound with the molecular formula C8H16O. It belongs to the class of cyclohexanol compounds and is characterized by a minty, camphor-like odor. This stable and versatile compound is commonly used in various industries due to its unique properties.

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  • 767-14-6 Structure
  • Basic information

    1. Product Name: (3R,5R)-3,5-dimethylcyclohexanol
    2. Synonyms: (1.alpha.,3.alpha.,5.beta.)-3,5-Dimethyl-cyclohexanol; (1alpha,3alpha,5beta)-3,5-Dimethylcyclohexanol; (3R,5R)-3,5-Dimethylcyclohexanol; cyclohexanol, 3,5-dimethyl-, (3R,5R)-
    3. CAS NO:767-14-6
    4. Molecular Formula: C8H16O
    5. Molecular Weight: 128.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 767-14-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 186.999°C at 760 mmHg
    3. Flash Point: 73.333°C
    4. Appearance: N/A
    5. Density: 0.894g/cm3
    6. Vapor Pressure: 0.18mmHg at 25°C
    7. Refractive Index: 1.452
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3R,5R)-3,5-dimethylcyclohexanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3R,5R)-3,5-dimethylcyclohexanol(767-14-6)
    12. EPA Substance Registry System: (3R,5R)-3,5-dimethylcyclohexanol(767-14-6)
  • 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: 767-14-6(Hazardous Substances Data)

767-14-6 Usage

Uses

Used in Flavor and Fragrance Industry:
(3R,5R)-3,5-dimethylcyclohexanol is used as a fragrance ingredient and flavoring agent for its distinct minty, camphor-like odor, adding unique scents and flavors to food and cosmetic products.
Used in Chemical Synthesis:
(3R,5R)-3,5-dimethylcyclohexanol is used as a solvent and intermediate in the production of other chemicals, taking advantage of its stable and versatile chemical structure for synthesizing a wide range of compounds.
Used in Organic Chemistry Research:
(3R,5R)-3,5-dimethylcyclohexanol serves as a valuable building block in organic chemistry research, contributing to the development of new methods and understanding of chemical reactions.
Used in Pharmaceutical Synthesis:
(3R,5R)-3,5-dimethylcyclohexanol is utilized in the synthesis of pharmaceuticals and other important chemicals, playing a crucial role in the development of new drugs and medicinal compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 767-14-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 767-14:
(5*7)+(4*6)+(3*7)+(2*1)+(1*4)=86
86 % 10 = 6
So 767-14-6 is a valid CAS Registry Number.

767-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-1r,3t-Dimethyl-cyclohexanol-(5)

1.2 Other means of identification

Product number -
Other names cis,trans-3,5-Dimethylcyclohexanol

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:767-14-6 SDS

767-14-6Relevant articles and documents

Transfer Hydrogenation of Ketones with (1-) as the Precatalyst

Bhaduri, Sumit,Sharma, Krishna,Mukesh, Doble

, p. 1191 - 1200 (2007/10/02)

The cluster 1a has been found to be an efficient precatalyst for the transfer hydrogenations of ketones and α,β-unsaturated ketones.With substrates such as (5S)-carvone , (3R)-methylcyclopentanone and (3R)-methylcyclohexanone, moderate to high diastereoselectivities were observed for reduction of the conjugated olefinic and ketonic functionalities respectively.Aromatisation of carvone to 5-isopropyl-2-methylphenol and disproportionation of cyclohex-2-en-1-one to phenol and cyclohexanone have also been found to be catalysed by 1a.Studies with radical inhibitors and other evidence suggest a radical mechanism for the transfer-hydrogenation and aromatisation reactions.In the transfer hydrogenation of cyclohex-2-en-1-one, the rate of conversion of 1a into other soluble species can be modelled accurately if autocatalysis is assumed.The time-dependent concentration profiles of cyclohex-2-en-1-one, cyclohexanone and cyclohexanol are simulated well if autocatalytic formation of an active intermediate followed by consecutive reactions leading to the formation of products is assumed.Such a model is also consistent with the proposed radical mechanism.

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