260782-41-0 Usage
Uses
Used in Pharmaceutical Industry:
Boc-ThionoPro-1-(6-nitro)benzotriazolide is used as a coupling reagent for the synthesis of peptides, facilitating the formation of peptide bonds with high efficiency and purity. Its protective Boc group ensures the selective deprotection of the amine functionality, which is crucial for the successful synthesis of complex peptide structures.
Used in Research Applications:
In research settings, Boc-ThionoPro-1-(6-nitro)benzotriazolide is employed as a key component in the development of novel peptide-based therapeutics and diagnostic agents. Its ability to enhance peptide bond formation and protect amine groups makes it a valuable asset in the exploration of new peptide sequences and their potential applications in medicine and biology.
Used in Solid-Phase Peptide Synthesis:
Boc-ThionoPro-1-(6-nitro)benzotriazolide is used as a critical reagent in solid-phase peptide synthesis, where it aids in the stepwise assembly of peptide chains on an insoluble support. Its contribution to the process ensures high yields and purity of the final peptide product, streamlining the production of peptides for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 260782-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,7,8 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 260782-41:
(8*2)+(7*6)+(6*0)+(5*7)+(4*8)+(3*2)+(2*4)+(1*1)=140
140 % 10 = 0
So 260782-41-0 is a valid CAS Registry Number.
260782-41-0Relevant academic research and scientific papers
Total Synthesis of the Cyclic Depsipeptide Vioprolide D via its (Z)-Diastereoisomer
Bach, Thorsten,Grab, Hanusch A.,Kirsch, Volker C.,Sieber, Stephan A.
supporting information, p. 12357 - 12361 (2020/05/05)
The first total synthesis of vioprolide D was accomplished in an overall yield of 2.0 % starting from methyl (2S)-3-benzyloxy-2-hydroxypropanoate (16 steps in the longest linear sequence). The cyclic depsipeptide was assembled from two building blocks of
Total synthesis of the cytotoxic cyclopeptide mollamide, isolated from the sea squirt Didemnum molle
McKeever, Benedict,Pattenden, Gerald
, p. 2701 - 2712 (2007/10/03)
Full details of a total synthesis of the novel reverse prenyl substituted cyclic peptide mollamide, isolated from the ascidian Didemnum molle, are described.
