36298-40-5 Usage
General Description
(S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate is a chemical compound with a complex structure consisting of a thiazolidine ring and a methyl group. It is commonly used in pharmaceutical and organic synthesis as a chiral building block for the production of various drugs and molecules. (S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate possesses unique stereochemical properties, making it a valuable reagent for the synthesis of enantiomerically pure compounds. Additionally, it has been studied for its potential biological activities, including antimicrobial, antifungal, and antioxidant properties, making it a promising candidate for drug development and research. Furthermore, (S)-methyl 2,2,5,5-tetramethyl-1,3-thiazolidine-4-carboxylate has shown potential as a reagent for the development of new synthetic methodologies and strategies in organic chemistry.
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 articles and documents
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.
