16947-86-7 Usage
Description
(S)-BOC-3-AMINO-2-(P-TOLUENESULFONYLAMINO)-PROPIONIC ACID, also known as Boc-Amino-PTS, is a chemical compound that serves as a crucial building block in the synthesis of peptides and pharmaceuticals. It is a derivative of (S)-2-Amino-3-(p-toluenesulfonamido)propionic acid and is widely recognized for its role in solid-phase peptide synthesis. Boc-Amino-PTS is an essential reagent for the protection of amino acids during peptide synthesis, ensuring the successful formation of the desired peptide sequences. This white to off-white crystalline powder should be stored in a cool, dry place away from light and moisture to maintain its stability and reactivity.
Uses
Used in Pharmaceutical Industry:
(S)-BOC-3-AMINO-2-(P-TOLUENESULFONYLAMINO)-PROPIONIC ACID is used as a key building block for the synthesis of various peptides and pharmaceuticals. Its application is primarily driven by its ability to protect amino acids during the peptide synthesis process, which is crucial for the successful creation of specific peptide sequences and the development of targeted therapeutic agents.
Used in Research and Development:
In the realm of research and development, Boc-Amino-PTS is employed as an important reagent for the protection of amino acids during peptide synthesis. This protection is vital for the accurate and efficient synthesis of complex peptide structures, which are often the focus of cutting-edge research in drug discovery and development. (S)-BOC-3-AMINO-2-(P-TOLUENESULFONYLAMINO)-PROPIONIC ACID's role in safeguarding amino acids allows researchers to explore new peptide-based therapeutic strategies and advance the field of peptide chemistry.
Used in Solid-Phase Peptide Synthesis:
(S)-BOC-3-AMINO-2-(P-TOLUENESULFONYLAMINO)-PROPIONIC ACID is used as a protective agent for amino acids in solid-phase peptide synthesis. This technique is a widely utilized method for the production of peptides, where Boc-Amino-PTS ensures the selective protection of amino groups, preventing unwanted side reactions and facilitating the stepwise assembly of the desired peptide sequence. Its application in this process is essential for the efficient and reliable synthesis of peptides with specific biological activities and potential pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16947-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,4 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16947-86:
(7*1)+(6*6)+(5*9)+(4*4)+(3*7)+(2*8)+(1*6)=147
147 % 10 = 7
So 16947-86-7 is a valid CAS Registry Number.
16947-86-7Relevant articles and documents
Asymmetric synthesis of (R)-6-amino-1-methyl-4-(3-methyl- benzyl)hexahydro-1H-1,4-diazepine from L-asparagine
Kato,Harada,Morie
, p. 1469 - 1478 (2007/10/03)
An efficient asymmetric synthesis of (R)-6-amino-1-methyl-4-(3- methylbenzyl)hexahydro-1H-1,4-diazepine [(R)-2] which serves as the amine part of (R)-1, a potent and selective 5-HT3 receptor antagonist, is described. Formation of the hexahydro-
Analogues of the cytostatic cyclic tetrapeptide chlamydocin, Synthesis of N41β-(N-maleoylglycyl) and N41β-(tert-butyloxycarbonyl) derivatives of cyclo (Gly-L-Phe-D-Pro-L-Dap)
Rich,Jasensky,Mueller,Anderson
, p. 567 - 572 (2007/10/02)
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