2503-29-9 Usage
Uses
Used in Pharmaceutical Research:
N-Cbz-DL-alanine amide is used as a key component in pharmaceutical research for the development of novel drug candidates. Its stability and compatibility with various reaction conditions facilitate the synthesis of complex peptide-based drugs.
Used in Peptide Synthesis:
In the field of peptide synthesis, N-Cbz-DL-alanine amide is employed as a building block for creating larger peptides and proteins. The presence of the carboxybenzyl (Cbz) protecting group ensures that the molecule remains stable and protected from unwanted reactions during the synthesis process.
Used in Chemical Modification:
N-Cbz-DL-alanine amide is utilized in chemical modification studies due to its versatility and ease of handling. Researchers can modify the compound to create new derivatives with potential applications in various industries.
Used in Drug Development Studies:
In drug development studies, N-Cbz-DL-alanine amide is used to explore its potential as a precursor for the creation of new pharmaceuticals. Its properties make it a promising candidate for the development of innovative treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 2503-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2503-29:
(6*2)+(5*5)+(4*0)+(3*3)+(2*2)+(1*9)=59
59 % 10 = 9
So 2503-29-9 is a valid CAS Registry Number.
2503-29-9Relevant academic research and scientific papers
A Stereoselective entry into functionalized 1,2-diamines by zinc-mediated homologation of α-aminoacids
Hoang, Cam Thuy,Alezra, Valerie,Guillot, Regis,Kouklovsky, Cyrille
, p. 2521 - 2524 (2008/02/05)
A general, stereoselective synthsis of 4,5-disubstituted imidazolidines-2-ones from α-aminoacids has been developed: the key steps are a Biaise reaction of bromoacetate on α-aminonitriles and further reduction. Although reduction with sodium cyanoborohydride afforded a mixture of cis and trans isomers 6a-e with moderate to good stereoselectivity, reduction with sodium in liquid ammonia gave the trans isomers 8a-e with complete stereoselectivity. Acidic hydrolysis of the urea gave 4-amino-pyrrolidinones, which can be precursors to β,γ-diaminoacids or 3-aminopyrrolidines.
