3-Acetyl-2-oxazolidinone - CAS 1432-43-5
Catalog: |
BB009526 |
Product Name: |
3-Acetyl-2-oxazolidinone |
CAS: |
1432-43-5 |
Synonyms: |
3-acetyl-1,3-oxazolidin-2-one |
IUPAC Name: | 3-acetyl-1,3-oxazolidin-2-one |
Description: | 3-Acetyl-2-oxazolidinone (CAS# 1432-43-5) is used as a reagent in the enantioselective synthesis of (+)-7-epigoniodiol, (-)-8-epigoniodiol, and (+)-9-deoxygoniopypyrone. Also a useful synthetic intermediate in the synthesis of 2-Oxazolone (O846555) which is a versatile tool for synthetic organic chemist. |
Molecular Weight: | 129.11 |
Molecular Formula: | C5H7NO3 |
Canonical SMILES: | CC(=O)N1CCOC1=O |
InChI: | InChI=1S/C5H7NO3/c1-4(7)6-2-3-9-5(6)8/h2-3H2,1H3 |
InChI Key: | COCHMAAUXSQMED-UHFFFAOYSA-N |
Boiling Point: | 282 °C at 760 mmHg |
Melting Point: | 69-71 °C (lit.) |
Purity: | 95 % |
Density: | 1.309 g/cm3 |
Appearance: | White to beige powder or crystals |
MDL: | MFCD00068820 |
LogP: | -0.07700 |
Publication Number | Title | Priority Date |
CN-111954692-A | Permeable superabsorbents and method for the production thereof | 20180410 |
CN-111278551-A | Super absorbent | 20171110 |
US-2020062714-A1 | BENZOIMIDAZOL-1,2-YL AMIDES AS Kv7 CHANNEL ACTIVATORS | 20161031 |
EP-3310329-A1 | Shaping keratin fibres using 2-oxazolidinone compounds | 20150618 |
JP-2018517750-A | Shaping of keratin fibers using 2-oxazolidinone compounds | 20150618 |
PMID | Publication Date | Title | Journal |
21589020 | 20101020 | 5-Hy-droxy-7-phenyl-5-(prop-2-yn-1-yl)-5,6-dihydro-1-benzofuran-2(4H)-one monohydrate | Acta crystallographica. Section E, Structure reports online |
18762314 | 20080901 | Removal of pharmaceutical compounds, nitroimidazoles, from waters by using the ozone/carbon system | Water research |
15704963 | 20050218 | 6-O-Benzyl- and 6-O-silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: effective glycosyl acceptors in the glucosamine 4-OH Series. effect of anomeric stereochemistry on the removal of the oxazolidinone group | The Journal of organic chemistry |
12207531 | 20020911 | Mechanism of the double aldol reaction: the first spectroscopic characterization of a carbon-bound boron enolate derived from carboxylic esters | Journal of the American Chemical Society |
Complexity: | 154 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 129.042593085 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 129.042593085 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 46.6 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.3 |
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