36298-40-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate is used as a chiral building block for the synthesis of various drugs and molecules. Its unique stereochemical properties make it a valuable reagent for creating enantiomerically pure compounds, which are essential in the development of effective and safe medications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate serves as a crucial component for the production of different molecules. Its complex structure and stereochemical properties allow for the creation of a wide range of compounds with specific functionalities and applications.
Used in Drug Development and Research:
(S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate is used as a promising candidate for drug development and research due to its potential biological activities. These include antimicrobial, antifungal, and antioxidant properties, which can be harnessed to develop new therapeutic agents and treatments for various diseases and conditions.
Used in the Development of New Synthetic Methodologies:
(S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate also serves as a reagent for the development of new synthetic methodologies and strategies in organic chemistry. Its complex structure and unique properties enable researchers to explore novel approaches and techniques in the synthesis of various compounds, further expanding the possibilities in chemical research and application.
Check Digit Verification of cas no
The CAS Registry Mumber 36298-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36298-40:
(7*3)+(6*6)+(5*2)+(4*9)+(3*8)+(2*4)+(1*0)=135
135 % 10 = 5
So 36298-40-5 is a valid CAS Registry Number.
36298-40-5Relevant academic research and scientific papers
D-Penicillamine and L-cysteine derived thiazolidine catalysts: an efficient approach to both enantiomers of secondary alcohols
Serra, M. Elisa Silva,Costa, Dora,Murtinho, Dina,Tavares, Nélia C.T.,Pinho e Melo, Teresa M.V.D.
, p. 5923 - 5927 (2016/09/07)
D-Penicillamine derived thiazolidine ligands were prepared in a two-step synthetic sequence and used in the enantioselective alkylation of a variety of aromatic aldehydes with diethylzinc at room temperature. Excellent ee, up to >99%, and nearly complete conversions were observed. Structurally analogous L-cysteine derived thiazolidine ligands were also synthesized and tested for comparative purposes, resulting in very good, albeit slightly lower selectivities, up to 89%. The combined use of these two types of thiazolidines constitutes a very interesting strategy for synthesizing both (S) and (R) enantiomers of chiral secondary alcohols, thus leading the way to a myriad of useful optically active products with opposite absolute configurations.
