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经验公式(希尔记法):
C3H3NO
化学文摘社编号:
分子量:
69.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-020-8
Beilstein/REAXYS Number:
103851
MDL number:
Assay:
98%
InChI key
ZCQWOFVYLHDMMC-UHFFFAOYSA-N
InChI
1S/C3H3NO/c1-2-5-3-4-1/h1-3H
SMILES string
c1cocn1
assay
98%
refractive index
n20/D 1.425 (lit.)
bp
69-70 °C (lit.)
mp
−87-−84 °C (lit.)
density
1.05 g/mL at 25 °C (lit.)
Quality Level
General description
恶唑是一大类杂环芳香化合物的母体分子。它是弱碱性的,可作为缺电子二烯用于Diels-Alder环加成反应。它可进行硝化、磺化、卤化、Friedel-Crafts烷化和酰化反应。
Application
噁唑可用于:
- 分子内Diels–Alder(IMDA)环加成反应合成天然产物
- 作为前体用于开环、亲核加成、再成环以及[2 + 2]、[3 + 2]和[4 + 2]环加成反应。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
66.2 °F - closed cup
flash_point_c
19 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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Oxazole derivatives are important medicinal compounds which are inhibitors of various enzymes such as NPP1, NPP2, NPP3, tyrosine kinase, dipeptidyl-peptidase IV, cyclooxygenase-2, and protein tyrosine phosphatase. In this study, an extensive range of new biologically active biphenyl oxazole derivatives was
Maryna V Kachaeva et al.
Computational biology and chemistry, 74, 294-303 (2018-04-27)
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Bo Pang et al.
Journal of the American Chemical Society, 142(25), 10931-10935 (2020-06-09)
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Lori M Culberson et al.
Physical chemistry chemical physics : PCCP, 16(9), 3964-3972 (2014-01-22)
Bond breaking is a challenging problem in both experimental and theoretical chemistry, due to the transient nature and multi-configurational electronic structure of dissociating molecules. We use anion photodetachment to probe the diradical interactions in the ring-opening reaction of oxazole and
J B Huppa et al.
The Journal of experimental medicine, 186(3), 393-403 (1997-08-04)
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