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151637

异噁唑

Name: 异噁唑
Brand: ALDRICH

99%

别名:

1,2-Oxazole, 1-Oxa-2-azacyclopentadiene, 2-Azafuran

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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:

288-14-2

分子量:

69.06

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849154

EC Number:

206-018-7

Beilstein/REAXYS Number:

103773

MDL number:

MFCD00003149

Assay:

99%

Form:

liquid

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属性

vapor density

2.4 (vs air)

Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.427 (lit.)

bp

93-95 °C (lit.)

density

1.078 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

c1cnoc1

InChI

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

InChI key

CTAPFRYPJLPFDF-UHFFFAOYSA-N

说明

General description

Isoxazole are described as inhibitors of acetylcholinesterase (AChE). Isoxazole ligands bind to and inhibit the Sxc- antiporter.

pictograms

GHS02

signalword

Danger

hcodes

H225

pcodes

P210

Hazard Classifications

Flam. Liq. 2

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

53.6 °F - closed cup

flash_point_c

12 °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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Deprotonation of Isoxazole: A Photoelectron Imaging Study.

Adam A Wallace et al.

The journal of physical chemistry. A, 124(38), 7768-7775 (2020-08-28)

We report a photoelectron imaging study of gas-phase deprotonation of isoxazole in which spectroscopic data are compared to the results of electronic structure calculations for the anion products corresponding to each of three possible deprotonation sites. The observed photoelectron spectra

Microwave accelerated synthesis of isoxazole hydrazide inhibitors of the system xc- transporter: Initial homology model.

Afnan A Matti et al.

Bioorganic & medicinal chemistry letters, 23(21), 5931-5935 (2013-09-18)

Microwave accelerated reaction system (MARS) technology provided a good method to obtain selective and open isoxazole ligands that bind to and inhibit the Sxc- antiporter. The MARS provided numerous advantages, including: shorter time, better yield and higher purity of the

Switchable Synthesis of Pyrroles and Pyrazines via Rh(II)-Catalyzed Reaction of 1,2,3-Triazoles with Isoxazoles: Experimental and DFT Evidence for the 1,4-Diazahexatriene Intermediate.

Nikolai V Rostovskii et al.

The Journal of organic chemistry, 82(1), 256-268 (2016-12-16)

4-Aminopyrrole-3-carboxylates and pyrazine-2-carboxylates were synthesized from 5-alkoxyisoxazoles and 1-sulfonyl-1,2,3-triazoles by tuning the Rh(II) catalyst and the reaction conditions. The reaction in chloroform at 100 °C under Rh

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全球贸易项目编号

货号	GTIN
151637-5G	04061838089823
151637-25G	04061838346155