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123214-39-1

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123214-39-1 Usage

General Description

4-Hydroxy-2,2-dimethylcyclohexanone, otherwise known as (4R)-4-hydroxy-2,2-dimethyl-3-oxacyclohexane, is a synthetic chemical compound. This chemical belongs to the family of cyclohexanones, which are compounds comprising a cyclohexane substituted by one or more ketone groups. 4-hydroxy-2,2-dimethylcyclohexanone possesses chiral center, indicating it has potential for use in creating chiral organic compounds. It commonly appears as a crystalline solid or powder. While not considered highly toxic, it should still be handled with standard safety precautions. Its uses range from applications in medical research to chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 123214-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,1 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 123214-39:
(8*1)+(7*2)+(6*3)+(5*2)+(4*1)+(3*4)+(2*3)+(1*9)=81
81 % 10 = 1
So 123214-39-1 is a valid CAS Registry Number.

123214-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2,2-dimethylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-2,2-dimethylcyclohexanone

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:123214-39-1 SDS

123214-39-1Relevant articles and documents

Enzymatic Preparation of Chiral 4-Hydroxy-2,2-dimethyl-1-cyclohexanone as a Chiral Building Block

Yamamoto, Hiroshi,Oritani, Takayuki,Koga, Hideo,Horiuchi, Tadao,Yamashita, Kyohei

, p. 1915 - 1921 (2007/10/02)

(S)-4-Hydroxy-2,2-dimethyl-1-cyclohexanone (1a) was prepared by two enzymatic methods. 1,4-Cyclohexanediol was converted to monoacetal (11) via (+/-)-1a.Enzymatic reduction of 11 by baker's yeast gave (S)-1 of almost 100 percent e.e.Direct hydroxylation of 2,2-dimethyl-1-cyclohexanone (14) by P-450 camphor monooxygenase of the cloned genes of Pseudomonas putida PpG1 gave (S)-1a of almost 100 percent e.e., too.According to Mitsunobu's method, SN-2 inversion of (S)-1 gave (R)-1.

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