5638-70-0

Basic information

• Product Name: [1,3]OXAZINANE-2,6-DIONE
• Synonyms: [1,3]OXAZINANE-2,6-DIONE;1,3-oxazinane-2,6-quinone
• CAS NO: 5638-70-0
• Molecular Formula: C4H5NO3
• Molecular Weight: 115.09
• Mol File: 5638-70-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Density: 1.33g/cm³
• Refractive Index: 1.459
• CAS DataBase Reference: [1,3]OXAZINANE-2,6-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: [1,3]OXAZINANE-2,6-DIONE(5638-70-0)
• EPA Substance Registry System: [1,3]OXAZINANE-2,6-DIONE(5638-70-0)

Safety Data

• Hazardous Substances Data: 5638-70-0(Hazardous Substances Data)

Usage

General Description

[1,3]Oxazinane-2,6-dione, also known as 1,3-diazanane-2,6-dione, is a chemical compound with the molecular formula C4H4N2O2. It is a cyclic organic compound containing a six-membered ring with oxygen and nitrogen atoms. [1,3]OXAZINANE-2,6-DIONE is used as a reagent in organic synthesis and as a building block for the creation of other chemical compounds. It has applications in the pharmaceutical and agrochemical industries, where it is used in the production of various drugs and pesticides. Additionally, [1,3]Oxazinane-2,6-dione has been studied for its potential biological activity, including anticancer and antibacterial properties.

InChI:InChI=1/C4H5NO3/c6-3-1-2-5-4(7)8-3/h1-2H2,(H,5,7)

Upstream product

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• 16690-93-0 sodium β-alaninate 
• 107-95-9 3-amino propanoic acid 

Downstream Products

• 40331-75-7 3-(2-nitro-phenylsulfanyl)-[1,3]oxazinane-2,6-dione 

Relevant articles and documents

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METHOD OF SYNTHESIZING N-CARBOXYANHYDRIDE USING FLOW REACTOR

PROBLEM TO BE SOLVED: To provide a synthesis method that allows high-yield continuous production of a compound of interest in synthesis and production of N-carboxyanhydride (NCA) and the like using a flow reactor. SOLUTION: In a synthesis method using a flow reactor 100, a basic solution adjusted in advance to a pH of 7-14 becomes acidic with a pH of 0-7, or an acidic solution adjusted in advance to a pH of 0-7 becomes basic with a pH of 7-14, within 60 seconds after the start of mixture of at least two ingredient solutions. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPOandINPIT

Simultaneous assembly of the β-lactam and thiazole moiety by a new multicomponent reaction

A novel multicomponent reaction of β-aminothiocarboxylic acids, aldehydes, and 3-dimethylamino-2-isocyanoacylate is described. During the course of this reaction two heterocyclic moieties, a thiazole and a β-lactam ring, are formed simultaneously and under mild conditions. The increase in molecular complexity here is dramatic as 2 C-N, 2 C-S and 1 C-C bonds are formed in a new 'one-pot' multicomponent reaction.