143415-63-8 Usage
Description
Boc-2-Methoxy-L-Phenylalanine is an unnatural amino acid derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. It is synthesized through the Pd-mediated C-C bond formation in tandem with 2-Methylpyridine.
Uses
Used in Pharmaceutical Industry:
Boc-2-Methoxy-L-Phenylalanine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of novel drugs with potential applications in treating different medical conditions.
Used in Chemical Research:
Boc-2-Methoxy-L-Phenylalanine serves as an important intermediate in chemical research, particularly in the field of organic synthesis. It can be utilized to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
In the field of material science, Boc-2-Methoxy-L-Phenylalanine can be employed as a component in the development of advanced materials with specific properties, such as improved stability or enhanced biocompatibility.
Used in Peptide Synthesis:
Boc-2-Methoxy-L-Phenylalanine is used as a non-natural amino acid in peptide synthesis, allowing for the creation of novel peptide sequences with potential applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 143415-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143415-63:
(8*1)+(7*4)+(6*3)+(5*4)+(4*1)+(3*5)+(2*6)+(1*3)=108
108 % 10 = 8
So 143415-63-8 is a valid CAS Registry Number.
143415-63-8Relevant articles and documents
Synthesis of chirally pure 2,5-disubstituted diketopiperazines derived from trisubstituted phenylalanines
Danthi, Satyavijayan Narasimhan,Hill, Ronald A.
, p. 835 - 844 (2007/10/03)
Some new chirally pure 2,5-substituted diketopiperazines were synthesized starting from 2-methoxybenzyl alcohol. This multistep synthesis proceeds through the enzymatic synthesis of chirally pure amino acids, protection and dipeptide coupling, cyclization of dipeptide ester formates, and nitration of the resulting diketopiperazines.
