147331-83-7 Usage
Description
2H-1,3-Thiazine-4-carboxylic acid, tetrahydro-, (4S)-(9CI) is a chiral chemical compound with the molecular formula C5H7NO2S. It is a derivative of thiazine and carboxylic acid, featuring a tetrahydro structure. 2H-1,3-Thiazine-4-carboxylicacid,tetrahydro-,(4S)-(9CI) is characterized by its specific stereochemistry, indicated by the (4S)-(9CI) designation. Due to its unique structure and properties, it holds potential in pharmaceuticals and organic synthesis, and may be utilized in the development of new drugs or as a component in chemical reactions. Further research and experimentation are required to determine its exact applications and properties.
Uses
Used in Pharmaceutical Industry:
2H-1,3-Thiazine-4-carboxylic acid, tetrahydro-, (4S)-(9CI) is used as a potential building block in the development of new drugs. Its unique structure and properties make it a promising candidate for pharmaceutical applications, where it could contribute to the creation of innovative therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 2H-1,3-Thiazine-4-carboxylic acid, tetrahydro-, (4S)-(9CI) serves as a valuable intermediate or reagent. Its specific stereochemistry and tetrahydro structure allow it to participate in various chemical reactions, facilitating the synthesis of complex organic compounds and contributing to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 147331-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147331-83:
(8*1)+(7*4)+(6*7)+(5*3)+(4*3)+(3*1)+(2*8)+(1*3)=127
127 % 10 = 7
So 147331-83-7 is a valid CAS Registry Number.
147331-83-7Relevant articles and documents
Preparations of Optically Active Homocysteine and Homocystine by Asymmetric Transformation of (RS)-1,3-Thiazane-4-carboxylic Acid
Miyazaki, Hideya,Ohta, Atsushi,Kawakatsu, Nobuyuki,Waki, Yukitaka,Gogun, Yasuhiro,et al.
, p. 536 - 540 (2007/10/02)
DL-Homocysteine from (RS)-homocysteine thiolactone hydrochloride was subjected to reaction with formaldehyde in acetic acid to give (RS)-1,3-thiazane-4-carboxylic acid monohydrate .An asymmetric transformation of (RS)-THA*H2O was achieved via salt formation with optically active tartaric acid in the presence of salicylaldehyde in acetic acid.The (R)- and (S)-THA obtained, respectively, from the salt of (R)-THA with (2R,3R)-tartaric acid and its enantiomeric salt were treated with hydroxylamine hydrochloride to give D- and L-Hcy of 100percent optical purity, respectively, in 50percent yield from (RS)-HTL*HCl.Oxidation of D- and L-Hcy with hydrogen peroxide gave D- and L-homocystine, respectively, in 47percent yield.