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Key Documents

O9409

Sigma-Aldrich

2-Oxazolidinone

98%

Synonym(s):

1,3-Oxazolidin-2-one, 2-Oxazolidone, 2-Oxo-1,3-oxazolidine, 2-Oxotetrahydro-1,3-oxazole

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About This Item

Empirical Formula (Hill Notation):
C3H5NO2
CAS Number:
Molecular Weight:
87.08
Beilstein:
106251
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

bp

220 °C/48 mmHg (lit.)

mp

83-87 °C (lit.)

SMILES string

O=C1NCCO1

InChI

1S/C3H5NO2/c5-3-4-1-2-6-3/h1-2H2,(H,4,5)

InChI key

IZXIZTKNFFYFOF-UHFFFAOYSA-N

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Application

2-Oxazolidinone can be employed as a precursor for the preparation of acryloyloxazolidin-2-ones , trans-3-cinnamoyloxazolidin-2-one, 3-bromo-2-oxazolidinone , 4-methoxy-2-oxazolidinone , coordination compound, tetrakis[μ-(2-oxazolidinonato-κN3:κO2)]tetra-, (4Cu-Cu).

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Photoinduced, copper-catalyzed alkylation of amides with unactivated secondary alkyl halides at room temperature
Do Hien-Quang, et al.
Journal of the American Chemical Society, 136(5), 2162-2167 (2014)
Nada A Al-Hasawi et al.
Anticancer research, 40(9), 5125-5140 (2020-09-04)
Neuroblastoma (NB), the most common extracranial malignant childhood tumor accounts for about 15% of cancer-related deaths in children. Despite the intensive treatment of patients with high-risk scarification of NB, clinical outcomes indicate tumor recurrence greater than 50% and late severe
Mathieu Esgulian et al.
Organic & biomolecular chemistry, 15(6), 1453-1462 (2017-01-21)
A number of cyclic derivatives of 3-amino-2,4-dihydroxybutanoic acid are known in the literature but they are often prepared from other cyclic precursors. This study showed that the title compound too may serve as a convenient substrate for cyclization reactions. Using
Stereocontrolled Synthesis of trans/cis-2, 3-Disubstituted Cyclopropane-1, 1-diesters and Applications in the Syntheses of Furanolignans
Shen Y, et al.
The Journal of Organic Chemistry, 83(20), 12549-12558 (2018)
Asymmetric Diels-Alder Reaction of α,β -Unsaturated Oxazolidin-2-one Derivatives Catalyzed by a Chiral Fe (III)-Bipyridine Diol Complex
Li Mao, et al.
Organic Letters, 20(4), 995-998 (2018)

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