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Merck
CN

230138

噁唑

98%

别名:

1,3-恶唑, 3-氮杂呋喃

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关于此项目

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:
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产品名称

噁唑, 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

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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。

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。

pictograms

FlameCorrosion

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
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Maryna V Kachaeva et al.
Computational biology and chemistry, 74, 294-303 (2018-04-27)
Based on modern literature data about biological activity of E7010 derivatives, a series of new sulfonamides as potential anticancer drugs were rationally designed by QSAR modeling methods Сlassification learning QSAR models to predict the tubulin polymerization inhibition activity of novel
Haseen Ahmad et al.
European journal of medicinal chemistry, 208, 112759-112759 (2020-09-05)
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
Bo Pang et al.
Journal of the American Chemical Society, 142(25), 10931-10935 (2020-06-09)
Nonribosomal peptide synthetase (NRPS) oxidase (Ox) domains oxidize protein-bound intermediates to install crucial structural motifs in bioactive natural products. The mechanism of this domain remains elusive. Here, by studying indigoidine synthetase, a single-module NRPS involved in the biosynthesis of indigoidine
Kristjan Bloudoff et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(1), 95-100 (2016-12-21)
Nonribosomal peptide synthetases (NRPSs) are a family of multidomain, multimodule enzymes that synthesize structurally and functionally diverse peptides, many of which are of great therapeutic or commercial value. The central chemical step of peptide synthesis is amide bond formation, which
Oxazole as an Electron-Deficient Diene in the Diels-Alder Reaction
Suarez-Moreno G, et al.
Organic Letters, 13, 6358-6361 (2011)

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