202390-86-1 Usage
Description
(2S,4S,5R)-3-Benzoyl-2-(p-methoxyphenyl)-4-phenyl-1,3-oxazolidine-5-carboxylic acid is a complex chiral molecule with a molecular structure that includes a benzoyl group, p-methoxyphenyl group, phenyl group, and oxazolidine-5-carboxylic acid group. It possesses three stereocenters, which may contribute to its unique structural features and functional groups.
Uses
Used in Pharmaceutical Applications:
(2S,4S,5R)-3-Benzoyl-2-(p-methoxyphenyl)-4-phenyl-1,3-oxazolidine-5-carboxylic acid is used as a potential pharmaceutical candidate due to its unique structural features and functional groups. Further research and studies are necessary to fully understand its chemical properties and potential uses in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 202390-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,3,9 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 202390-86:
(8*2)+(7*0)+(6*2)+(5*3)+(4*9)+(3*0)+(2*8)+(1*6)=101
101 % 10 = 1
So 202390-86-1 is a valid CAS Registry Number.
202390-86-1Relevant articles and documents
Preparation method of side chain of paclitaxel
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Paragraph 0040; 0041; 0043; 0044; 0045; 0046, (2018/11/22)
The invention discloses a preparation method of a side chain of paclitaxel shown as a formula II. The preparation method includes the following steps that in a solvent, under the temperature not higher than an atmospheric boiling point of the solvent, a c
Total asymmetric synthesis of taxol by dehydration condensation between 7-TES baccatin III and protected N-benzoylphenylisoserines prepared by enantioselective aldol reaction
Shiina, Isamu,Saitoh, Katsuyuki,Frechard-Ortuno, Isabelle,Mukaiyama, Teruaki
, p. 3 - 4 (2007/10/03)
Total asymmetric synthesis of Taxol was completed by dehydration condensation between a protected N-benzoylphenylisoserine 4 or 9 and 7-TES baccatin in which was prepared from 8-membered ring enone. Taxol side chains 4, 7, 9 and 11, optically active protected N-benzoylphenylisoserines, were successfully synthesized by enantioselective aldol reaction from two achiral starting materials, benzaldehyde and an enol silyl ether derived from S-ethyl benzyloxyethanethioate.
