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230138

Sigma-Aldrich

Oxazol

98%

Synonym(e):

1,3-Oxazole, 3-Azafuran

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About This Item

Empirische Formel (Hill-System):
C3H3NO
CAS-Nummer:
288-42-6
Molekulargewicht:
69.06
Beilstein:
103851
EG-Nummer:
206-020-8
MDL-Nummer:
MFCD00009751
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24853776
NACRES:
NA.22

Assay

98%

Brechungsindex

n20/D 1.425 (lit.)

bp

69-70 °C (lit.)

mp (Schmelzpunkt)

−87-−84 °C (lit.)

Dichte

1.05 g/mL at 25 °C (lit.)

SMILES String

c1cocn1

InChI

1S/C3H3NO/c1-2-5-3-4-1/h1-3H

InChIKey

ZCQWOFVYLHDMMC-UHFFFAOYSA-N

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Allgemeine Beschreibung

Oxazole is the parent molecule for a large class of heterocyclic aromatic compounds. It is a weak base that can be used as an electron-deficient diene in the Diels-Alder cycloaddition reaction. It undergoes nitration, sulfonation, halogenation, Friedel-Crafts alkylation, and acylation.

Zubehör

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

FlameCorrosion
GHS02,GHS05

Signalwort

Danger

H-Sätze

H225,H318

Gefahreneinstufungen

Eye Dam. 1 - Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

66.2 °F - closed cup

Flammpunkt (°C)

19 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCQ2873
MKCM9663
MKCK6799
MKCH1019
MKBX4478V

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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
Dawid Siodłak et al.
The journal of physical chemistry. B, 118(9), 2340-2350 (2014-02-18)
Oxazole ring occurs in numerous natural peptides, but conformational properties of the amino acid residue containing the oxazole ring in place of the C-terminal amide bond are poorly recognized. A series of model compounds constituted by the oxazole-amino acids occurring
Ilya Lyagin et al.
Molecules (Basel, Switzerland), 24(13) (2019-06-30)
Mycotoxins are highly dangerous natural compounds produced by various fungi. Enzymatic transformation seems to be the most promising method for detoxification of mycotoxins. This review summarizes current information on enzymes of different classes to convert various mycotoxins. An in-depth analysis
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
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