206559-98-0 Usage
General Description
3-(N,N-Dimethylamino)-D-alanine is a chemical compound that belongs to the class of amino acids. It contains a dimethylamino group attached to the carbon atom of the alanine molecule. 3-(N,N-Dimethylamino)-D-alanine is most commonly used in the field of medicinal chemistry and drug discovery, as it has potential applications in the synthesis of peptide-based drugs and pharmaceuticals. The dimethylamino group in 3-(N,N-Dimethylamino)-D-alanine can also confer unique properties to the compound, making it useful for studying the structure-activity relationships of peptides and proteins. Additionally, this compound may have potential applications in the development of new biomaterials and as a tool for investigating protein-protein interactions. Further research and exploration of 3-(N,N-Dimethylamino)-D-alanine's properties and applications may reveal its full potential in the field 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 articles and documents
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).
