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(S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is a chemical compound characterized by the molecular formula C13H23NO4S. It is an amino acid derivative featuring a pyrrolidine ring and a carboxylic acid group. (S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is notable for its tert-butoxycarbonyl (Boc) group, which serves as a protective agent for the amine functionality, and the methylthio group, which introduces a sulfur atom into the molecule. This unique structure and its properties render it a versatile building block in the synthesis of pharmaceuticals and other bioactive molecules, making it a valuable asset in organic chemistry.

1093063-64-9

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1093063-64-9 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is used as a key building block for the development of various pharmaceuticals. Its incorporation into the molecular structure of drugs enhances their bioactivity and pharmacological properties, contributing to the creation of more effective medications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is utilized as an intermediate for the preparation of complex organic compounds. Its unique structural features facilitate the synthesis of a wide range of molecules with diverse applications, from pharmaceuticals to agrochemicals.
Used in Bioactive Molecule Development:
(S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is also employed in the development of bioactive molecules. Its structural components can be manipulated to create novel compounds with specific biological activities, potentially leading to the discovery of new therapeutic agents or other useful bioactive substances.
Used in Research and Development:
(S)-1-(tert-butoxycarbonyl)-3-(methylthio)pyrrolidine-3-carboxylic acid is frequently used in research and development settings to study the effects of structural modifications on the properties and reactivity of amino acid derivatives. Understanding these relationships can lead to the design of more efficient synthetic routes and the development of new compounds with improved characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1093063-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,0,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1093063-64:
(9*1)+(8*0)+(7*9)+(6*3)+(5*0)+(4*6)+(3*3)+(2*6)+(1*4)=139
139 % 10 = 9
So 1093063-64-9 is a valid CAS Registry Number.

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