1262886-64-5 Usage
Uses
Used in Organic Chemistry:
(S)-N-Fmoc-2-(7'-octenyl)glycine is used as a building block in the synthesis of peptides and proteins for various applications in the field of organic chemistry.
Used in Pharmaceutical Industry:
(S)-N-Fmoc-2-(7'-octenyl)glycine is used as a key intermediate in the development of novel bioactive peptides and pharmaceuticals, contributing to the advancement of drug discovery and therapeutics.
Used in Protein Engineering:
(S)-N-Fmoc-2-(7'-octenyl)glycine is used as a modifying agent in protein engineering to study and manipulate the structure and function of proteins, enabling the design of proteins with specific properties and functions.
Used in Solid-Phase Peptide Synthesis:
(S)-N-Fmoc-2-(7'-octenyl)glycine is used as a protected amino acid in solid-phase peptide synthesis, where the Fmoc group protects the amino group during the synthesis process, facilitating the stepwise assembly of peptide chains.
Check Digit Verification of cas no
The CAS Registry Mumber 1262886-64-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,8,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1262886-64:
(9*1)+(8*2)+(7*6)+(6*2)+(5*8)+(4*8)+(3*6)+(2*6)+(1*4)=185
185 % 10 = 5
So 1262886-64-5 is a valid CAS Registry Number.
1262886-64-5Relevant academic research and scientific papers
Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides
Aillard, Boris,Robertson, Naomi S.,Baldwin, Adam R.,Robins, Siobhan,Jamieson, Andrew G.
supporting information, p. 8775 - 8782 (2014/12/11)
The efficient asymmetric synthesis of unnatural alkenyl amino acids required for peptide 'stapling' has been achieved using alkylation of a fluorine-modified NiII Schiff base complex as the key step.
