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1,3-Cyclohexanediol,1-methyl-4-(1-methylethyl)-,[1R-(1alpha,3alpha,4alpha)]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193286-34-9

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193286-34-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 20 hydrogen (H) atoms, and 2 oxygen (O) atoms.

Explanation

The CAS (Chemical Abstracts Service) number is a unique identifier assigned to a specific chemical compound, which helps in its identification and search in databases.

Explanation

This describes the arrangement of atoms in the molecule, including the positions of the functional groups (diol, methyl, and isopropyl groups) and the stereochemistry (1R configuration).

Explanation

The compound contains two hydroxyl (OH) groups, making it a diol. Additionally, it has a methyl (-CH3) and an isopropyl (-CH(CH3)2) group attached to the cyclohexane ring.

Explanation

It is an organic compound, which means it primarily consists of carbon and hydrogen atoms, along with other elements like oxygen.

Explanation

Due to its unique structure, 1,3-Cyclohexanediol,1-methyl-4-(1-methylethyl)-,[1R-(1alpha,3alpha,4alpha)]-(9CI) can be used as a starting material for the synthesis of other organic chemicals and pharmaceuticals.

Explanation

The compound may also be used in the production of polymers and other industrial products due to its chemical properties.

Explanation

The compound's structure and properties may make it a candidate for further research in the medical field, possibly leading to new drug discoveries.

Explanation

The specific uses and properties of 1,3-Cyclohexanediol,1-methyl-4-(1-methylethyl)-,[1R-(1alpha,3alpha,4alpha)]-(9CI) may vary depending on the manufacturer and the intended applications for which it is being used.

Chemical Structure

1,3-Cyclohexanediol, 1-methyl-4-(1-methylethyl)-, [1R-(1alpha,3alpha,4alpha)]-

Functional Groups

Diol, Methyl, Isopropyl

Type of Compound

Organic Chemical

Applications

Precursor in the synthesis of various organic chemicals and pharmaceuticals

Potential Applications

Manufacturing of polymers and other industrial products

Biological Activity

May have potential uses in medical research and drug development

Variation in Uses and Properties

Depends on manufacturers and intended applications

Check Digit Verification of cas no

The CAS Registry Mumber 193286-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,8 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 193286-34:
(8*1)+(7*9)+(6*3)+(5*2)+(4*8)+(3*6)+(2*3)+(1*4)=159
159 % 10 = 9
So 193286-34-9 is a valid CAS Registry Number.

193286-34-9SDS

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 (1R,3R,4R)-1-hydroxy neoisomenthol

1.2 Other means of identification

Product number -
Other names 1,3-Cyclohexanediol,1-methyl-4-(1-methylethyl)-,[1R-(1alpha,3alpha,4alpha)]-

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:193286-34-9 SDS

193286-34-9Downstream Products

193286-34-9Relevant academic research and scientific papers

Enantioselective preparation of 1-hydroxy neoisopulegol and 1-hydroxy neoisomenthol

Fkyerat, Abdellatif,Tabacchi, Raffaele

, p. 2231 - 2236 (2007/10/03)

A enantioselective procedure is described for the preparation of (1R,3R,4R)-1-hydroxy isopulegol 3 and (1R,3S,4R)-1-hydroxy neoisopulegol 4 in 4 steps starting from geraniol. Their enantiomers (1S,3S,4S)-1-hydroxy isopulegol 5 and (1R,3S,4R)-1-hydroxy neo

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