123214-39-1 Usage
Description
4-Hydroxy-2,2-dimethylcyclohexanone, also known as (4R)-4-hydroxy-2,2-dimethyl-3-oxacyclohexane, is a synthetic chemical compound belonging to the family of cyclohexanones. These compounds consist of a cyclohexane ring substituted by one or more ketone groups. 4-Hydroxy-2,2-dimethylcyclohexanone has a chiral center, which makes it a potential candidate for creating chiral organic compounds. It is typically found as a crystalline solid or powder and, while not highly toxic, should be handled with standard safety precautions.
Uses
Used in Medical Research:
4-hydroxy-2,2-dimethylcyclohexanone is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its chiral center allows for the creation of enantiomers, which can have different biological activities and are essential in drug development.
Used in Chemical Industries:
4-hydroxy-2,2-dimethylcyclohexanone is used as a building block for the production of other organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of various chemical products, including fragrances, dyes, and specialty chemicals.
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.
123214-39-1Relevant 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.
