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A16254

Sigma-Aldrich

2-Furyl methyl ketone

99%

Sinonimo/i:

2-Acetylfuran

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About This Item

Formula empirica (notazione di Hill):
C6H6O2
Numero CAS:
1192-62-7
Peso molecolare:
110.11
Beilstein:
107909
Numero CE:
214-757-1
Numero MDL:
MFCD00003242
Codice UNSPSC:
12352100
ID PubChem:
24890568
NACRES:
NA.22

Livello qualitativo

100

Saggio

99%

Stato

liquid

Indice di rifrazione

n20/D 1.5070 (lit.)

P. ebollizione

67 °C/10 mmHg (lit.)

Punto di fusione

26-28 °C (lit.)

Densità

1.098 g/mL at 25 °C (lit.)

Stringa SMILE

CC(=O)c1ccco1

InChI

1S/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H3
IEMMBWWQXVXBEU-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H300 + H330,H311,H319

Classi di pericolo

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Eye Irrit. 2

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

159.8 °F - closed cup

Punto d’infiammabilità (°C)

71 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
STBK6922
STBK0297
STBJ3962
STBH4523
STBG5217V

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5-Methylfurfural analytical standard

Supelco

91307

5-Methylfurfural

5-idrossimetil-2-furaldeide 99%

Sigma-Aldrich

H40807

5-idrossimetil-2-furaldeide

3-Acetyl-2,5-dimethylfuran 98%

Sigma-Aldrich

302694

3-Acetyl-2,5-dimethylfuran

2-Acetylpyrrole ReagentPlus®, 99%

Sigma-Aldrich

247359

2-Acetylpyrrole

2-Acetyl-5-methylfuran ≥98%, FG

Sigma-Aldrich

W360902

2-Acetyl-5-methylfuran

T R Bailey et al.
Journal of medicinal chemistry, 37(24), 4177-4184 (1994-11-25)
As a probe of the 3-methylisoxazole portion of our broad-spectrum antipicornaviral series, a panel of 2-acetylfuran analogues was prepared as replacements for the 3-methylisoxazole ring. Comparison of the two series showed remarkable similarity in potency, spectrum of activity, logP, and
Yu Wang et al.
Journal of agricultural and food chemistry, 56(24), 11997-12001 (2008-12-19)
Sugar type is a major factor regulating the reaction rates and pathways in Maillard reaction. Ribose and glucose were used to compare their reactivities and pathways of 2-acetylfuran formation. A stable isotope labeling method was used to study their reactivity.
T Kawai et al.
International archives of occupational and environmental health, 63(4), 285-291 (1991-01-01)
The concentrations of 2,5-hexanedione (2,5-HD), an n-hexane metabolite, and 2-acetylfuran (2-AF) were measured in urine samples from 123 workers who had predominantly been exposed to n-hexane vapor and 53 workers who had experienced no exposure to solvents. The time-weighted average
Thomas Magauer et al.
Organic letters, 13(20), 5584-5587 (2011-10-01)
A 9-step synthetic route to the complex carbohydrate methyl α-trioxacarcinoside B from 2-acetylfuran is described. Anomerically activated forms, including 1-phenylthio, 1-O-(4'-pentenyl), 1-fluoro, and 1-O-acetyl derivatives are also prepared.
Sulekh Chandra et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(4-5), 1347-1351 (2006-08-22)
Co(II), Ni(II) and Cu(II) complexes are synthesized with thiosemicarbazone (L1) and semicarbazone (L2) derived from 2-acetyl furan. These complexes are characterized by elemental analysis, molar conductance, magnetic susceptibility measurements, mass, IR, electronic and EPR spectral studies. The molar conductance measurements
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