501653-63-0 Usage
Uses
Used in Pharmaceutical Industry:
Glycine, N-[(4-fluorophenyl)methyl]-, ethyl ester is used as a building block for the synthesis of various drugs and molecules, due to its specific properties and potential applications in drug development and research.
Used in Medicinal Chemistry:
Glycine, N-[(4-fluorophenyl)methyl]-, ethyl ester is used as a chemical compound in medicinal chemistry, where it may have potential uses in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
Glycine, N-[(4-fluorophenyl)methyl]-, ethyl ester is used as a chemical compound in organic synthesis, where it may be utilized in the creation of new organic molecules and compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 501653-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,6,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 501653-63:
(8*5)+(7*0)+(6*1)+(5*6)+(4*5)+(3*3)+(2*6)+(1*3)=120
120 % 10 = 0
So 501653-63-0 is a valid CAS Registry Number.
501653-63-0Relevant academic research and scientific papers
Base-promoted c→n acyl rearrangement: An unconventional approach to α-amino acid derivatives
Ugarriza, Iratxe,Uria, Uxue,Carrillo, Luisa,Vicario, Jose L.,Reyes, Efraim
, p. 11650 - 11654 (2014/10/15)
We have discovered that N-alkyl aminomalonates undergo a fast and selective intramolecular C→N acyl rearrangement reaction in the presence of a strong base, leading to N-protected glycinates in excellent yield. Moreover, the fact that the reaction proceeds through a nucleophilic enolate intermediate has been used for implementing a tandem rearrangement/alkylation sequence that has been applied to the preparation of synthetically relevant nonproteinogenic tertiary and quaternary N-alkyl α-amino acids in a very simple and reliable way.
