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2,4-Oxazolidinedione

2,4-Oxazolidinedione is an organic compound with the formula HN(CO)2OCH2. It is a white solid. The parent ring is not particularly important, but this core structure is found in a variety anticonvulsant drugs. The parent compound is obtained by treating chloroacetamide with bicarbonate.[2]

2,4-Oxazolidenedione
Names
Preferred IUPAC name
1,3-Oxazolidine-2,4-dione
Other names
2,4-Oxazolidenedione
Identifiers
  • 2346-26-1 Y
3D model (JSmol)
  • Interactive image
ChemSpider
  • 87905 Y
  • 97389
UNII
  • R22D15229R Y
  • DTXSID60894083
  • InChI=1S/C3H3NO3/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6) Y
    Key: COWNFYYYZFRNOY-UHFFFAOYSA-N Y
  • InChI=1S/C3H3NO3/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
  • Key: COWNFYYYZFRNOY-UHFFFAOYSA-N
  • O=C1NC(=O)OC1
Properties
C3H3NO3
Molar mass 101.061 g·mol−1
Appearance white solid
Melting point 89–90 °C (192–194 °F; 362–363 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

See also edit

References edit

  1. ^ Traube, Wilhelm; Ascher, Richard (1913). "Über das Isohydantoin 2-Imino-4-keto-tetrahydro-oxazol und seine Homologen" [About the isohydantoin (?) of 2-imino-4-keto-tetrahydro-oxazole and its homologues]. Berichte der Deutschen Chemischen Gesellschaft (in German). 46 (2): 2077–2084. doi:10.1002/cber.191304602124.
  2. ^ Cesa, Stefania; Mucciante, Vittoria; Rossi, Leucio (1999). "Tetraethylammonium hydrogen carbonate in organic synthesis: Synthesis of oxazolidine-2,4-diones". Tetrahedron. 55: 193–200. doi:10.1016/S0040-4020(98)01025-4.

oxazolidinedione, organic, compound, with, formula, 2och2, white, solid, parent, ring, particularly, important, this, core, structure, found, variety, anticonvulsant, drugs, parent, compound, obtained, treating, chloroacetamide, with, bicarbonate, dimethadione. 2 4 Oxazolidinedione is an organic compound with the formula HN CO 2OCH2 It is a white solid The parent ring is not particularly important but this core structure is found in a variety anticonvulsant drugs The parent compound is obtained by treating chloroacetamide with bicarbonate 2 Dimethadione Ethadione Paramethadione Trimethadione2 4 Oxazolidenedione Names Preferred IUPAC name 1 3 Oxazolidine 2 4 dione Other names 2 4 Oxazolidenedione Identifiers CAS Number 2346 26 1 Y 3D model JSmol Interactive image ChemSpider 87905 Y PubChem CID 97389 UNII R22D15229R Y CompTox Dashboard EPA DTXSID60894083 InChI InChI 1S C3H3NO3 c5 2 1 7 3 6 4 2 h1H2 H 4 5 6 YKey COWNFYYYZFRNOY UHFFFAOYSA N YInChI 1S C3H3NO3 c5 2 1 7 3 6 4 2 h1H2 H 4 5 6 Key COWNFYYYZFRNOY UHFFFAOYSA N SMILES O C1NC O OC1 Properties Chemical formula C 3H 3N O 3 Molar mass 101 061 g mol 1 Appearance white solid Melting point 89 90 C 192 194 F 362 363 K Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox referencesSee also editGlycine N carboxyanhydride the parent 2 5 oxazolidinedioneReferences edit Traube Wilhelm Ascher Richard 1913 Uber das Isohydantoin 2 Imino 4 keto tetrahydro oxazol und seine Homologen About the isohydantoin of 2 imino 4 keto tetrahydro oxazole and its homologues Berichte der Deutschen Chemischen Gesellschaft in German 46 2 2077 2084 doi 10 1002 cber 191304602124 Cesa Stefania Mucciante Vittoria Rossi Leucio 1999 Tetraethylammonium hydrogen carbonate in organic synthesis Synthesis of oxazolidine 2 4 diones Tetrahedron 55 193 200 doi 10 1016 S0040 4020 98 01025 4 nbsp This anticonvulsant related article is a stub You can help Wikipedia by expanding it vte nbsp This article about a heterocyclic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title 2 4 Oxazolidinedione amp oldid 1092363522, wikipedia, wiki, book, books, library,

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