212650-44-7 Usage
Uses
Used in Organic Synthesis:
4-Benzyl-morpholine-3-carboxylic acid methyl ester is used as a key intermediate for the synthesis of complex organic molecules, facilitating the creation of new chemical entities with diverse properties and functions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Benzyl-morpholine-3-carboxylic acid methyl ester is utilized as a precursor in the development of novel drugs, contributing to the discovery of compounds with potential therapeutic effects.
Used in Drug Discovery and Development:
4-Benzyl-morpholine-3-carboxylic acid methyl ester is employed as a building block in drug discovery, enabling the synthesis of pharmacologically active compounds that can be further optimized for medicinal applications.
Used in Medicinal Chemistry:
This ester is used as a versatile component in medicinal chemistry, where it can be modified and combined with other molecules to create new drugs with improved efficacy, selectivity, and safety profiles.
Overall, 4-Benzyl-morpholine-3-carboxylic acid methyl ester is a valuable compound in the fields of organic chemistry and pharmaceuticals, with its applications spanning from the synthesis of new molecules to the development of innovative therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 212650-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,5 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 212650-44:
(8*2)+(7*1)+(6*2)+(5*6)+(4*5)+(3*0)+(2*4)+(1*4)=97
97 % 10 = 7
So 212650-44-7 is a valid CAS Registry Number.
InChI:InChI=1S/C13H17NO3/c1-16-13(15)12-10-17-8-7-14(12)9-11-5-3-2-4-6-11/h2-6,12H,7-10H2,1H3
212650-44-7Relevant academic research and scientific papers
Preparation method of chiral N-tert-butyloxycarborylmorpholine-3-carboxylic acid
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, (2020/08/25)
The invention provides a preparation method of chiral N-tert-butyloxycarborylmorpholine-3-carboxylic acid, which comprises the following steps: (1) carrying out an amino protection reaction on chiralserinamide and an amino protective agent to obtain a com
