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151637

Sigma-Aldrich

Isoxazol

99%

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C3H3NO
CAS-Nummer:
288-14-2
Molekulargewicht:
69.06
Beilstein:
103773
EG-Nummer:
206-018-7
MDL-Nummer:
MFCD00003149
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24849154
NACRES:
NA.22

Dampfdichte

2.4 (vs air)

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.427 (lit.)

bp

93-95 °C (lit.)

Dichte

1.078 g/mL at 25 °C (lit.)

Lagertemp.

2-8°C

SMILES String

c1cnoc1

InChI

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

InChIKey

CTAPFRYPJLPFDF-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Piktogramme

Flame
GHS02

Signalwort

Danger

H-Sätze

H225

P-Sätze

P210

Gefahreneinstufungen

Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

53.6 °F - closed cup

Flammpunkt (°C)

12 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

03205

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Sigma-Aldrich

724637

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Dimethylsulfit 99%

Sigma-Aldrich

108618

Dimethylsulfit

4-Oxazolcarboxaldehyd 97%

Sigma-Aldrich

697915

4-Oxazolcarboxaldehyd

Pyridazin 98%

Sigma-Aldrich

P57204

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Sigma-Aldrich

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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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