127062-02-6 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Dioxolane-4-carboxylic acid, 2,2,5-trimethyl, (4S-trans)-(9CI) is used as a building block or intermediate for the synthesis of other compounds in the pharmaceutical industry. Its specific chemical structure and functional groups may contribute to the development of new drugs or drug candidates with potential therapeutic applications.
Used in Chemical Synthesis:
1,3-Dioxolane-4-carboxylic acid, 2,2,5-trimethyl, (4S-trans)-(9CI) is used as a chemical intermediate in the synthesis of various organic compounds. Its unique structure and functional groups can be utilized in the preparation of complex molecules, potentially leading to the discovery of new materials or chemical entities with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 127062-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,6 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127062-02:
(8*1)+(7*2)+(6*7)+(5*0)+(4*6)+(3*2)+(2*0)+(1*2)=96
96 % 10 = 6
So 127062-02-6 is a valid CAS Registry Number.
127062-02-6Relevant articles and documents
Total synthesis of (-)-Jiadifenin
Yang, Yang,Fu, Xingnian,Chen, Jianwei,Zhai, Hongbin
, p. 9825 - 9828 (2012)
As easy as ABCD: (-)-Jiadifenin was synthesized in eighteen reaction steps from 1-[(E)-(4′-bromo-2′-butenyl)oxy]-4-methoxybenzene. Key features of this synthesis include: 1) Ireland-Claisen rearrangement to produce the two contiguous quaternary centers at
A Selective Baeyer-Villiger Oxidation: A Total Synthesis of (-)-Acetomycin
Ziegler, Frederick E.,Kim, Hakwon
, p. 7669 - 7672 (2007/10/02)
A short, stereoselective synthesis of (-)-acetomycin (2) from L-threonine is reported.The final step in the synthesis is a selective Baeyer-Villiger oxidation that discriminates between two methyl ketones.
ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS
Pottie, M.,Eycken, J. Van der,Vandewalle, M.,Dewanckele, J. M.,Roeper, H.
, p. 5319 - 5322 (2007/10/02)
2,2-dimethyl-1,3-dioxolane-4-carboxylic acid derived chiral building blocks were prepared from substituted α,β-unsaturated acids with high enantiomeric purities by enzymatic hydrolysis of their n.butyl esters.
