791782-11-1 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(S)-Benzyl 2-amino-3-methoxypropanoate is used as a building block for the development of new pharmaceuticals, leveraging its structural resemblance to natural amino acids to create novel drug candidates.
Used in Organic Synthesis:
(S)-Benzyl 2-amino-3-methoxypropanoate serves as a synthetic intermediate for the creation of various organic compounds, contributing to the advancement of chemical research and development.
Used in Biochemical Studies:
(S)-Benzyl 2-amino-3-methoxypropanoate is utilized as a research tool in biochemical studies, potentially aiding in the understanding of amino acid interactions and functions within biological systems.
Used in Chemical Biology and Medicinal Chemistry:
(S)-Benzyl 2-amino-3-methoxypropanoate is employed as a research molecule in the fields of chemical biology and medicinal chemistry, where it may contribute to the discovery of new biological activities and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 791782-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,7,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 791782-11:
(8*7)+(7*9)+(6*1)+(5*7)+(4*8)+(3*2)+(2*1)+(1*1)=201
201 % 10 = 1
So 791782-11-1 is a valid CAS Registry Number.
791782-11-1Relevant academic research and scientific papers
Process for the preparation of Lacosamide including resolution of O-methyl-DL-serine
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Page/Page column 12-13, (2012/08/28)
The present invention provides a process for the preparation of lacosamide in substantially optically pure form, which in one aspect comprises the following steps: (i) resolution of O-methyl-D,L-serine to provide O-methyl-D-serine in substantially optically pure form; (ii) acetylation of O-methyl-D-serine thereby obtained to provide the N-acetyl derivative thereof in substantially optically pure form; (iii) activating the carboxy group of the compound thereby obtained; and (iv) reacting the compound thereby obtained with benzylamine.
PROCESS FOR PREPARING LACOSAMIDE
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Page/Page column 22, (2012/06/01)
The present invention provides a process for the preparation of lacosamide in substantially optically pure form, which in one aspect comprises the following steps: (i) resolution of O-methyl-D,L-serine to provide O-methyl-D-serine in substantially optically pure form; (ii) acetylation of O-methyl-D-serine thereby obtained to provide the N-acetyl 10 derivative thereof in substantially optically pure form; (iii) activating the carboxy group of the compound thereby obtained; and (iv) reacting the compound thereby obtained with benzylamine.
