| Weight | 69.063 g/mol |
|---|---|
| Formula | C3H3NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
OXAZOLE (288-42-6)
Score:
#2027 in Physics
,
#2537 in Biochemistry
,
#6318 in Chemistry
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- From Peptide Precursors to Oxazole and Thiazole-Containing Peptide Antibiotics: Microcin B17 Synthase (Science, 1996)
- Recent Advances in the Total Syntheses of Oxazole-Containing Natural Products (Tetrahedron, 2004)
- Thiazole and oxazole peptides: biosynthesis and molecular machinery. (Natural Product Reports, 1999)
- Cyclization of Propargylic Amides: Mild Access to Oxazole Derivatives (Chemistry: A European Journal, 2010)
- Fluorescence Detection of Specific Sequence of Nucleic Acids by Oxazole Yellow-Linked Oligonucleotides. Homogeneous Quantitative Monitoring of In Vitro Transcription (Nucleic Acids Research, 1996)
- Metal-free, organocatalytic cascade formation of CN and CO bonds through dual sp3 CH activation: oxidative synthesis of oxazole derivatives (Chemical Communications, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=COC=N1
-
InChIKeyZCQWOFVYLHDMMC-UHFFFAOYSA-N
- Pubchem - OXAZOLE
- Wikipedia - oxazole
Oxazole is the parent compound for a vast class of heterocyclic aromatic organic compounds. These are azoles with an oxygen and a nitrogen separated by one carbon. Oxazoles are aromatic compounds but less so than the thiazoles.
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benzo[d]oxazol-6-amine
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1-Methylpyrrole
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OXAZOLE
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