160885-24-5 Usage
Uses
Used in Peptide Synthesis:
(S)-3-(benzylamino)-2-(benzyloxycarbonylamino)propanoic acid is used as a building block in peptide synthesis for the creation of novel peptides with specific functions and properties. Its incorporation into peptide sequences allows for the development of bioactive peptides with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-3-(benzylamino)-2-(benzyloxycarbonylamino)propanoic acid is used as a key intermediate in the synthesis of peptidomimetics. These synthetic compounds have the potential to exhibit improved pharmacokinetic properties, such as enhanced stability, bioavailability, and reduced immunogenicity compared to natural peptides. Peptidomimetics can be designed to target specific biological receptors or enzymes, making them valuable for the development of new drugs for various therapeutic areas, including neurological disorders and other diseases.
Used in Research and Development:
(S)-3-(benzylamino)-2-(benzyloxycarbonylamino)propanoic acid is used as a research tool in the field of chemistry and medicine. Its unique structure and properties make it an interesting compound for studying the interactions between peptides and their target molecules, as well as for exploring new methods of peptide synthesis and modification. This research can contribute to the advancement of our understanding of peptide-based therapeutics and the development of new drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 160885-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160885-24:
(8*1)+(7*6)+(6*0)+(5*8)+(4*8)+(3*5)+(2*2)+(1*4)=145
145 % 10 = 5
So 160885-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O4/c21-17(22)16(12-19-11-14-7-3-1-4-8-14)20-18(23)24-13-15-9-5-2-6-10-15/h1-10,16,19H,11-13H2,(H,20,23)(H,21,22)/t16-/m0/s1
160885-24-5Relevant articles and documents
Reaction of Trimethylsilylamines with N-Cbz-L-Serine-β-Lactone: A Convenient Route to Optically Pure β-Amino-L-alanine Derivatives
Ratemi, Elaref S.,Vederas, John C.
, p. 7605 - 7608 (2007/10/02)
Trimethylsilylamines, Me3Si-NR2, react with N-Cbz-L-serine-β-lactone in acetonitrile primarily by alkyl oxygen cleavage of the lactone ring to give optically pure N-Cbz-β-amino-L-alanine derivatives in good yields.Use of halogenated sovents such as chloro
