206559-98-0 Usage
Uses
Used in Medicinal Chemistry and Drug Discovery:
3-(N,N-Dimethylamino)-D-alanine is utilized as a key component in the synthesis of peptide-based drugs and pharmaceuticals, leveraging its distinctive structural features to enhance the therapeutic efficacy of these compounds.
Used in the Study of Structure-Activity Relationships:
In the field of peptide and protein research, 3-(N,N-Dimethylamino)-D-alanine serves as a valuable tool for investigating the structure-activity relationships of biologically active peptides and proteins, providing insights into their function and potential applications.
Used in the Development of Biomaterials:
3-(N,N-Dimethylamino)-D-alanine is employed in the creation of innovative biomaterials, where its unique properties may contribute to the development of advanced materials with specific biological interactions and functions.
Used in Investigating Protein-Protein Interactions:
As a research tool, 3-(N,N-Dimethylamino)-D-alanine aids in the exploration of protein-protein interactions, which is crucial for understanding complex biological processes and the design of targeted therapeutic interventions.
Further exploration and research into the properties and applications of 3-(N,N-Dimethylamino)-D-alanine are expected to uncover its full potential, particularly in the realms of chemical and biomedical research.
Check Digit Verification of cas no
The CAS Registry Mumber 206559-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,5,5 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 206559-98:
(8*2)+(7*0)+(6*6)+(5*5)+(4*5)+(3*9)+(2*9)+(1*8)=150
150 % 10 = 0
So 206559-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O2/c1-7(2)3-4(6)5(8)9/h4H,3,6H2,1-2H3,(H,8,9)/t4-/m1/s1
206559-98-0Relevant academic research and scientific papers
ASYMMERTIC SYNTHESIS OF Β-SUBSTITUTED α-AMINO ACIDS VIA A CHIRAL Ni(II) COMPLEX OF DEHYDROALANINE
Belokon, , Yuri N.,Sagyan, Ashot S.,Djamgaryan, Silva M.,Bakhmutov, Vladimir I.,Belikov, Vasili M.
, p. 5507 - 5514 (2007/10/02)
An efficient approach to the asymmetric synthesis of β-substituted (S)-alanines is describen.The chiral Ni(II) complex of a Schiff base derived from (S)-o-N-(N-benzylpropyl)aminobenzophenone (BBP) and glycine was treated with formaldehyde and sodium methoxide to give a corresponding (R)-serine complex which, in turn, was converted to the chiral Ni(II) dehydroalanine complex.Michael type base catalyzed addition of nucleophiles (including MeOH, Me2NH, PhCH2NH2, imidazole, PhSH, PhCH2SH,, malonic ester and benzylmagnesium chloride) produced a mixture of diastereoisomeric complexes with a 70-90percent excess of S,S (or L,L) isomers over the S,R (or L,D) ones.The cleavage of pure diastereoisomers with aqueous HCl gave, in good yields, β-substituted (S) (or L)-alanines and regenerated the chiral auxiliary (BBP).
