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Merck
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Key Documents

Altri documenti

151637

Sigma-Aldrich

Isoxazole

99%

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C3H3NO
Numero CAS:
288-14-2
Peso molecolare:
69.06
Beilstein:
103773
Numero CE:
206-018-7
Numero MDL:
MFCD00003149
Codice UNSPSC:
12352100
ID PubChem:
24849154
NACRES:
NA.22

Densità del vapore

2.4 (vs air)

Livello qualitativo

200

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.427 (lit.)

P. eboll.

93-95 °C (lit.)

Densità

1.078 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

c1cnoc1

InChI

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

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Categorie correlate

Descrizione generale

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

Pittogrammi

Flame
GHS02

Avvertenze

Danger

Indicazioni di pericolo

H225

Consigli di prudenza

P210

Classi di pericolo

Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

53.6 °F - closed cup

Punto d’infiammabilità (°C)

12 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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N-Ethylbutylamine ≥98.0%

Sigma-Aldrich

03205

N-Ethylbutylamine

4-Bromoisoxazole 95%

Sigma-Aldrich

724637

4-Bromoisoxazole

Dimethyl sulfite 99%

Sigma-Aldrich

108618

Dimethyl sulfite

4-Oxazolecarboxaldehyde 97%

Sigma-Aldrich

697915

4-Oxazolecarboxaldehyde

Pyridazine 98%

Sigma-Aldrich

P57204

Pyridazine

3-Aminoisoxazole 95%

Sigma-Aldrich

424218

3-Aminoisoxazole

Margarita Gutiérrez et al.
The Journal of pharmacy and pharmacology, 65(12), 1796-1804 (2013-11-05)
Inhibition of acetylcholinesterase (AChE) is a common treatment for early stages of Alzheimer's disease. In this study, nine isoxazoles derivatives were tested for their in-vitro AChE activity. The molecular docking showed the interaction of the compounds with the active site.
Mingxing Wang et al.
Journal of molecular graphics & modelling, 84, 18-28 (2018-05-25)
Studies on human genetics have implicated the voltage-gated sodium channel Nav1.7 as an appealing target for the treatment of pain. In this study, we put forward a ligand-based pharmacophore for the first time, which was generated by a set of
Marina N Semenova et al.
ACS combinatorial science, 20(12), 700-721 (2018-11-20)
A series of both novel and reported combretastatin analogues, including diarylpyrazoles, -isoxazoles, -1,2,3-triazoles, and -pyrroles, were synthesized via improved protocols to evaluate their antimitotic antitubulin activity using in vivo sea urchin embryo assay and a panel of human cancer cells.
Adam A Wallace et al.
The journal of physical chemistry. A, 125(1), 317-326 (2020-12-29)
Electron capture by the σ* LUMO of isoxazole triggers the dissociation of the O-N bond and the opening of the ring. Photodetachment of the resulting anion accesses a neutral structure, in which the O· and ·N bond fragments interact through
Sahaya Asirvatham et al.
Anti-inflammatory & anti-allergy agents in medicinal chemistry, 14(2), 128-137 (2015-08-13)
A series of newer 3-(4'-methoxyphenyl)-5-substituted phenylisoxazoles derivatives have been synthesized by reacting hydroxylamine hydrochloride with chalcones. The chalcones were formed by reacting different aromatic aldehydes with 4-methoxyacetophenone in presence of aqueos potassium hydroxide (KOH). The purity of all the synthesized
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