1037301-10-2 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-amino-tetrahydro-furan-3-carboxylic acid butyl ester (S)-mandelic acid is used as an intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its unique molecular structure and potential biological activity make it a valuable component in the development of new drugs and molecular compounds for a range of therapeutic applications.
Used in Chemical Industry:
In the chemical industry, (S)-3-amino-tetrahydro-furan-3-carboxylic acid butyl ester (S)-mandelic acid is utilized as a key component in the production of chiral compounds. Its distinctive molecular structure allows for the creation of enantiomerically pure substances, which are essential in various chemical reactions and processes.
Overall, (S)-3-amino-tetrahydro-furan-3-carboxylic acid butyl ester (S)-mandelic acid is a versatile compound with significant potential in both the pharmaceutical and chemical industries, contributing to the development of innovative drugs, molecular compounds, and chiral substances for a wide array of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1037301-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,3,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1037301-10:
(9*1)+(8*0)+(7*3)+(6*7)+(5*3)+(4*0)+(3*1)+(2*1)+(1*0)=92
92 % 10 = 2
So 1037301-10-2 is a valid CAS Registry Number.
1037301-10-2Relevant academic research and scientific papers
PROCESS FOR THE SYNTHESIS OF DERIVATIVES OF 3-AMINO-TETRAHYDROFURAN-3-CARBOXYLIC ACID AND USE THEREOF AS MEDICAMENTS
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Page/Page column 61; 88; 92-93; 94-95, (2008/12/07)
The present invention relates to a process for the manufacturing of substituted 3- amino-tetrahydrofuran-3-carboxylic acid amides of general formula (I) and their precursors in high optical purity to the precursors of the synthesis of substituted S-Amino-tetrahydrofuran-S-carboxylic acid amides of general formula (I) in high optical purity, and to the tautomers, enantiomers, diastereomers, mixtures and salts of substituted 3-amino- tetrahydrofuran-3-carboxylic acid amides of general formula (I) in high optical purity, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, which have valuable properties.
