162932-23-2 Usage
Description
Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI), also known as (R)-Methyl 2,2,2-trifluoro-1-(2,2-dimethyl-1,3-dioxolan-4-yl)ethanone, is a chiral chemical compound with a distinctive molecular structure. It features a trifluoromethyl group and a dioxolane ring, which contribute to its unique properties and potential for selective reactions. Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI)'s stereochemistry as the (R)-enantiomer is crucial for its specific applications in asymmetric synthesis and drug discovery.
Uses
Used in Organic Synthesis:
Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI) is utilized as a reagent in organic synthesis, taking advantage of its chiral nature and the unique properties of its trifluoromethyl group. This allows for the creation of complex molecules with high selectivity and specificity.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI) serves as an intermediate in the production of various drugs. Its chiral structure and the potential for selective reactions make it a valuable component in the synthesis of enantiomerically pure compounds, which are essential for the development of effective and safe medications.
Used in Asymmetric Synthesis:
Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI) is employed in asymmetric synthesis processes, where the (R)-enantiomer's stereochemistry plays a critical role. This enables the production of enantiomerically pure compounds, which are often necessary for biological activity and to avoid potential side effects associated with the presence of both enantiomers.
Used in Drug Discovery:
Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI)'s unique molecular structure and chiral properties make it a valuable tool in drug discovery. Ethanone, 1-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2,2-trifluoro-, (R)(9CI) can be used to explore new chemical spaces and identify potential drug candidates with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 162932-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162932-23:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*2)+(2*2)+(1*3)=132
132 % 10 = 2
So 162932-23-2 is a valid CAS Registry Number.
