5840-77-7 Usage
Also Known As
Methionine sulfone
Type of Compound
Cyclic amino acid derivative
Common Uses
Building block for synthesis of pharmaceuticals and biologically active compounds
Properties
Antimicrobial: Exhibits antimicrobial properties
Antioxidant: Displays antioxidant properties
Anti-inflammatory: Shows anti-inflammatory effects
Applications
Medicine: Studied for potential medical applications
Agriculture: Investigated for potential agricultural uses
Potential Uses
Dietary Supplement: Explored as a dietary supplement for overall health
Treatment of Inflammatory Diseases: Potential applications in treating inflammatory conditions
Check Digit Verification of cas no
The CAS Registry Mumber 5840-77-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5840-77:
(6*5)+(5*8)+(4*4)+(3*0)+(2*7)+(1*7)=107
107 % 10 = 7
So 5840-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO3S/c1-11-3-2-4-5(8)10-6(9)7-4/h4H,2-3H2,1H3,(H,7,9)
5840-77-7Relevant articles and documents
A new simple and quantitative synthesis of α-aminoacid-N-carboxyanhydrides (oxazolidines-2,5-dione)
Collet, Helene,Bied, Catherine,Mion, Louis,Taillades, Jacques,Commeyras, Auguste
, p. 9043 - 9046 (2007/10/03)
Nitrosation of chiral N-carbamoylaminoacids with a mixture of NO and O2 gives, with the same configuration and in quantitative yield the corresponding α-aminoacid-N-carboxyanhydrides (NCA), well known precursors of peptides. The by products of this reaction are N2 and H2O. Copyright (C) 1996 Elsevier Science Ltd.
ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.
Hosten, N.,Anteunis, M. J. O.
, p. 45 - 47 (2007/10/02)
Apparent separation of 1.1 or higher on Chiralsil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.
