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4-[2-(methylthio)ethyl]oxazolidine-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5840-77-7

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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)

5840-77-7Downstream Products

5840-77-7Relevant academic research and scientific papers

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.

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