

Available forms:Colorless to light yellow liquid
pd_proNo:526387-0c170357-12d2-4ccf-a21b-8da06a5d8952
pd_productuse:
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Definition |
ChEBI: 2-acetylfuran is a furan carrying an acetyl substituent at the 2-position. Used in the production of the antibiotic cefuroxime (CHEBI:3515). It is a member of furans, a methyl ketone and an aromatic ketone. |
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Preparation |
2-Acetylfuran is synthesized from furan and acetyl chloride by a Friedel–Kraft condensation. |
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Aroma threshold values |
Detection: 10 ppm |
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General Description |
2-Furyl methyl ketone is a volatile heterocyclic flavor compound that may be formed in food due to Maillard reaction. It has been reported in roasted sesame seeds, fried beef and sweet corn products. |
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Health Hazard |
Exposures to 2-acetylfuran by ingestion, inhalation, and skin absorption cause harmful effects. It causes irritation to the skin, the eyes, coughing, respiratory tract irritation, and respiratory distress. Accidental ingestion causes irritation of the digestive tract. There are no data about chronic exposure and adverse effects. |
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storage |
2-Acetylfuran should be kept away from sources of ignition, heat, sparks, flame, and light. It should be kept stored in a tightly sealed container in a dry area/refrigerated (below 4°C/39°F). |
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Precautions |
During handling and use of 2-acetylfuran, occupational workers should use appropriate and proper personal protective equipment and wear a self-contained breathing apparatus. Workers should avoid generating dusty conditions, minimize generation and accumulation of dust, remove all sources of ignition, and use a spark-proof tool. Workers should use 2-acetylfuran only in a chemical fume hood. |
InChI:InChI=1/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H3
Rhodium and iridium diolefin catalysts f...
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Levulinic acid and its esters participat...
Reactivity in enantioselective oxidation...
Isomers of 1-(2-furyl)-methyl-3-buten-ol...
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The use of a wet alumina/potassium ferra...
Many reports claim the existence of athe...
The well-defined iron PNP pincer complex...
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D-Fructose
GLUTATHIONE
Thiophene-2-thiol
Tetrahydrothiophen-3-one
2-ethylthiophene
2-Methylpyrazine
5-Methylfurfural
2-thiophenethanol
1-(2-furyl)-1-ethanone
2-methylthiophene-3-thiol
2-Acetylpyrrole
2-methylfuran-3-thiol
| Conditions | Yield |
|---|---|
|
In
water;
at 160 ℃;
for 2h;
pH=7.5;
|
D-glucose
GLUTATHIONE
1,3-thiazole
Thiophene-2-thiol
Tetrahydrothiophen-3-one
furfural
2,5-DIMETHYLTHIOPHENE
5-Methylfurfural
1-(2-furyl)-1-ethanone
2-methylthiophene-3-thiol
2-Acetylpyrrole
2-methylfuran-3-thiol
| Conditions | Yield |
|---|---|
|
In
water;
at 160 ℃;
for 2h;
pH=7.5;
|
diazomethane
furfural
furan
acetic anhydride
2-furan-2-yl-hexan-2-ol
2-acetylfuran-2-furoylhydrazone
(E)-N'-(1-(furan-2-yl)ethylidene)isonicotinic hydrazide
2-(2-furyl)-6-methyl-4-quinolinecarboxylic acid
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