289910-65-2 Usage
Uses
Used in Organic Chemistry:
Boc-Tyr(tBu)-Pro-OH is used as a building block for the synthesis of peptides and small molecules, facilitating the construction of complex organic structures with precision and control over the reactive sites.
Used in Peptide Synthesis:
In the field of peptide synthesis, Boc-Tyr(tBu)-Pro-OH is utilized as a protected amino acid, allowing chemists to incorporate it into peptide chains with the assurance that the Boc group will protect the tyrosine's hydroxyl group from side reactions until it is ready to be deprotected.
Used in Pharmaceutical Development:
Boc-Tyr(tBu)-Pro-OH is employed in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs, where its protective groups ensure the stability and correct formation of the desired peptide sequences.
Used in Research and Development:
In research settings, Boc-Tyr(tBu)-Pro-OH is used as a component in the exploration of new chemical reactions and the synthesis of novel compounds, providing a controlled environment for studying the reactivity and properties of protected amino acids.
Check Digit Verification of cas no
The CAS Registry Mumber 289910-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,9,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 289910-65:
(8*2)+(7*8)+(6*9)+(5*9)+(4*1)+(3*0)+(2*6)+(1*5)=192
192 % 10 = 2
So 289910-65-2 is a valid CAS Registry Number.
289910-65-2Relevant articles and documents
β-Casomorphins: Substitution of phenylalanine with β-homo phenylalanine increases the μ-type opioid receptor affinity
Longobardo, Luigi,Melck, Dominique,Siciliano, Rosa,Santini, Antonello,Marzo, Vincenzo Di,Cammarota, Giancarlo
, p. 1185 - 1188 (2007/10/03)
Two analogues of bovine β-casomorphin-7 and β-casomorphin-5 containing a β-homo phenylalanine in substitution of the phenylalanine in position 3 were synthesised and tested for their μ-opioid receptor affinity. The modification enhanced the μ receptor affinity 5-fold in the case of modified β-CM-7 and 2-fold for modified β-CM-5 when compared to the natural peptides. (C) 2000 Elsevier Science Ltd. All rights reserved.
