2-Acetylfuran

Available forms:Colorless to light yellow liquid

pd_proNo:526387-0c170357-12d2-4ccf-a21b-8da06a5d8952

pd_productuse:

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Detailed introduction

Top Quality 2-Acetylfuran 1192-62-7 Hot Sell In Stock

  • Molecular Formula:C6H6O2
  • Molecular Weight:110.112
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.772mmHg at 25°C 
  • Melting Point:26-28 °C 
  • Refractive Index:1.507 
  • Boiling Point:183.4 °C at 760 mmHg 
  • Flash Point:160 °F 
  • PSA:30.21000 
  • Density:1.098 g/mL at 25 °C 
  • LogP:1.48220 

2-Acetylfuran(Cas 1192-62-7) Usage

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.

Preparation

2-Acetylfuran is synthesized from furan and acetyl chloride by a Friedel–Kraft condensation.

Aroma threshold values

Detection: 10 ppm

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.

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.

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).

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

1192-62-7 Relevant articles

Preparation and Degradation of Rhodium and Iridium Diolefin Catalysts for the Acceptorless and Base-Free Dehydrogenation of Secondary Alcohols

Buil, Mariá L.,Collado, Alba,Esteruelas, Miguel A.,G? mez-Gallego, Mar,Izquierdo, Susana,Nicasio, Antonio I.,Onìate, Enrique,Sierra, Miguel A.

, p. 989 - 1003 (2021)

Rhodium and iridium diolefin catalysts f...

-

Hartough,Kosak

, p. 1012 (1947)

-

-

Hartough,Kosak

, p. 3093,3095 (1947)

-

Selective oxidation of alcohols in the presence of an Os/O2-system

D?bler, Christian,Mehltretter, Gerald M,Sundermeier, Uta,Eckert, Markus,Militzer, Hans-Christian,Beller, Matthias

, p. 8447 - 8449 (2001)

The osmium-catalyzed oxidation of alcoho...

Comparison of 2-acetylfuran formation between ribose and glucose in the Maillard reaction

Wang, Yu,Ho, Chi-Tang

, p. 11997 - 12001 (2008)

Sugar type is a major factor regulating ...

Copper-Catalyzed Stille Cross-Coupling Reaction and Application in the Synthesis of the Spliceostatin Core Structure

Ghosh, Arun K.,Born, Joshua R.,Veitschegger, Anne M.,Jurica, Melissa S.

, p. 8111 - 8120 (2020)

An efficient palladium-free Stille cross...

-

Hartough,Kosak

, p. 867 (1948)

-

Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap

Wise, Nicola J.,Williams, Jonathan M.J.

, p. 3639 - 3641 (2007)

Levulinic acid and its esters participat...

Enantioselective microbial oxidation of 1-arylethanol in an organic solvent

Nakamura, Kaoru,Inoue, Yuko,Ohno, Atsuyoshi

, p. 4375 - 4376 (1994)

Reactivity in enantioselective oxidation...

Rearrangements of some furan and benzofuran 1,5,-dienols

Martin,Wurster,Boylan,Borzilleri,Engel,Walsh

, p. 8395 - 8398 (1993)

Isomers of 1-(2-furyl)-methyl-3-buten-ol...

-

Hartough,Kosak

, p. 2639 (1946)

-

-

Gol'dfarb,Danjuschewskii

, (1963)

-

Potassium ferrate on wet alumina: Preparation and reactivity

Caddick,Murtagh,Weaving

, p. 9365 - 9373 (2000)

The use of a wet alumina/potassium ferra...

Examining of athermal effects in microwave-induced glucose/glycine reaction and degradation of polysaccharide from Porphyra yezoensis

Zhou, Cunshan,Yu, Xiaojie,Ma, Haile,Liu, Shulan,Qin, Xiaopei,Yagoub, Abu El-Gasim A.,Owusu, John

, p. 38 - 44 (2013)

Many reports claim the existence of athe...

Iron–PNP-Pincer-Catalyzed Transfer Dehydrogenation of Secondary Alcohols

Budweg, Svenja,Wei, Zhihong,Jiao, Haijun,Junge, Kathrin,Beller, Matthias

, (2019)

The well-defined iron PNP pincer complex...

Characteristic flavor formation of thermally processed N-(1-deoxy-α-D-ribulos-1-yl)-glycine: Decisive role of additional amino acids and promotional effect of glyoxal

Zhan, Huan,Cui, Heping,Yu, Junhe,Hayat, Khizar,Wu, Xian,Zhang, Xiaoming,Ho, Chi-Tang

, (2021/09/28)

The role of amino acids and α-dicarbonyl...

Hydration of Alkynes to Ketones with an Efficient and Practical Polyoxomolybdate-based Cobalt Catalyst

Xie, Ya,Wang, Jingjing,Wang, Yunyun,Han, Sheng,Yu, Han

, p. 4985 - 4989 (2021/10/12)

Hydration of alkynes to ketones is one o...

Visible-light photocatalytic selective oxidation of C(sp3)-H bonds by anion-cation dual-metal-site nanoscale localized carbon nitride

Duan, Limei,Li, Peihe,Li, Wanfei,Liu, Jinghai,Liu, Ying,Liu, Zhifei,Lu, Ye,Sarina, Sarina,Wang, Jinghui,Wang, Yin,Wang, Yingying,Zhu, Huaiyong

, p. 4429 - 4438 (2021/07/12)

Selective oxidation of C(sp3)-H bonds to...

Selective oxidation of alkenes to carbonyls under mild conditions

Huo, Jie,Xiong, Daokai,Xu, Jun,Yue, Xiaoguang,Zhang, Pengfei,Zhang, Yilan

supporting information, p. 5549 - 5555 (2021/08/16)

Herein, a practical and sustainable meth...

1192-62-7 Process route

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D-Fructose

GLUTATHIONE
70-18-8

GLUTATHIONE

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2-ethylthiophene

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109-08-0

2-Methylpyrazine

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620-02-0

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5402-55-1

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1-(2-furyl)-1-ethanone
1192-62-7,80145-44-4

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2-methylthiophene-3-thiol
2527-76-6

2-methylthiophene-3-thiol

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1072-83-9

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2-methylfuran-3-thiol
28588-74-1

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Conditions
Conditions Yield
In water; at 160 ℃; for 2h; pH=7.5;
D-glucose
50-99-7

D-glucose

GLUTATHIONE
70-18-8

GLUTATHIONE

1,3-thiazole
288-47-1

1,3-thiazole

Thiophene-2-thiol
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Tetrahydrothiophen-3-one
1003-04-9

Tetrahydrothiophen-3-one

furfural
98-01-1

furfural

2,5-DIMETHYLTHIOPHENE
638-02-8

2,5-DIMETHYLTHIOPHENE

5-Methylfurfural
620-02-0

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1-(2-furyl)-1-ethanone
1192-62-7,80145-44-4

1-(2-furyl)-1-ethanone

2-methylthiophene-3-thiol
2527-76-6

2-methylthiophene-3-thiol

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1072-83-9

2-Acetylpyrrole

2-methylfuran-3-thiol
28588-74-1

2-methylfuran-3-thiol

Conditions
Conditions Yield
In water; at 160 ℃; for 2h; pH=7.5;

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