10138-99-5 Usage
Uses
Used in Pharmaceutical Applications:
(2S)-2-Amino-3-dimethylaminopropanoic acid is used as a therapeutic agent for its antimicrobial and antiviral properties, offering potential treatments for various infections and diseases caused by microorganisms.
Used in Neurological Treatments:
In the field of neurology, (2S)-2-Amino-3-dimethylaminopropanoic acid is utilized as a potential treatment for neurological disorders, suggesting its capacity to influence or ameliorate certain neurological conditions.
Used in Organic Synthesis:
(2S)-2-Amino-3-dimethylaminopropanoic acid is employed as a chiral building block in organic synthesis, playing a crucial role in the creation of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical processes.
Used in Research and Development:
In the scientific community, (2S)-2-Amino-3-dimethylaminopropanoic acid is used as a subject of study to further understand its properties, potential applications, and mechanisms of action, contributing to the advancement of medical and chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 10138-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10138-99:
(7*1)+(6*0)+(5*1)+(4*3)+(3*8)+(2*9)+(1*9)=75
75 % 10 = 5
So 10138-99-5 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-/m0/s1
10138-99-5Relevant 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).
