1097192-06-7 Usage
Uses
Used in Peptide Chemistry:
2S-[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino-7-octynoic acid is used as a building block in peptide chemistry for the synthesis of complex peptides and proteins. Its unique structure allows for the creation of novel peptide sequences with enhanced properties, such as increased stability, solubility, and bioactivity.
Used in Drug Development:
In the pharmaceutical industry, 2S-[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino-7-octynoic acid is utilized as a key component in the development of new drugs. Its chemical versatility enables the design of innovative drug candidates with improved pharmacokinetic and pharmacodynamic profiles, potentially leading to more effective treatments for various diseases.
Used in Bioconjugation:
2S-[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino-7-octynoic acid is employed as a bioconjugation agent to modify and enhance the properties of proteins and peptides for therapeutic or research purposes. Its ability to form stable covalent bonds with biomolecules allows for the development of targeted drug delivery systems, imaging agents, and biosensors with enhanced performance.
Used in the Study of Protein-Protein Interactions:
The unique structure of 2S-[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino-7-octynoic acid makes it a valuable tool for investigating protein-protein interactions and binding mechanisms. By incorporating 2S-{[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino}-7-octynoic acid into protein constructs, researchers can gain insights into the molecular basis of protein recognition and develop strategies to modulate these interactions for therapeutic benefit.
Used in the Synthesis of Complex Molecules:
2S-[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino-7-octynoic acid serves as a versatile building block in the synthesis of complex molecules for a variety of scientific and technological applications. Its chemical properties enable the creation of novel compounds with tailored properties, such as improved stability, selectivity, and reactivity, which can be applied in areas such as materials science, catalysis, and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 1097192-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,1,9 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1097192-06:
(9*1)+(8*0)+(7*9)+(6*7)+(5*1)+(4*9)+(3*2)+(2*0)+(1*6)=167
167 % 10 = 7
So 1097192-06-7 is a valid CAS Registry Number.
1097192-06-7Relevant articles and documents
Nα-Fmoc-protected ω-azido- and ω-alkynyl-L- amino acids as building blocks for the synthesis of "clickable" peptides
Isaad, Alexandra Le Chevalier,Barbetti, Francesca,Rovero, Paolo,D'Ursi, Anna Maria,Chelli, Mario,Chorev, Michael,Papini, Anna Maria
, p. 5308 - 5314 (2008)
The growing interest in the 1,4-disubstituted-1,2,3-triazolyl moiety as an amide bond surrogate and its formation through very mild, chemoselective, and bioorthogonal CuI-catalyzed Huisgen 1,3-dipolar [3+2] cycloaddition of an alkynyl to an azi
