Passa al contenuto
Merck
Tutte le immagini(1)

Key Documents

View All Documentation

151637

Sigma-Aldrich

Isoxazole

99%

Sinonimo/i:

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

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

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)

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

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCF5673
BCCF2945
BCCF2946
BCCF2968
BCCD7852

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 6

1 of 6

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
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.