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O9409

Sigma-Aldrich

2-Oxazolidinone

98%

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Synonym(s):
1,3-Oxazolidin-2-one, 2-Oxazolidone, 2-Oxo-1,3-oxazolidine, 2-Oxotetrahydro-1,3-oxazole
Empirical Formula (Hill Notation):
C3H5NO2
CAS Number:
Molecular Weight:
87.08
Beilstein/REAXYS Number:
106251
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

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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1 of 4

This Item
228001450669450693
vibrant-m

O9409

2-Oxazolidinone

vibrant-m

228001

3-Methyl-2-oxazolidinone

assay

98%

assay

99.5%

assay

98%

assay

98%

form

solid

form

liquid

form

-

form

-

mp

83-87 °C (lit.)

mp

15 °C (lit.)

mp

86-87 °C (lit.)

mp

65-68 °C (lit.)

bp

220 °C/48 mmHg (lit.)

bp

87-90 °C/1 mmHg (lit.)

bp

-

bp

-

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

13 - Non Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Cysteine-Aminoethylation-Assisted Chemical Ubiquitination of Recombinant Histones
Chu G-C, et al.
Journal of the American Chemical Society, 141(8), 3654-3663 (2019)
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)
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

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