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2-Acetylfuran structure, CAS 1192-62-7

2-Acetylfuran

CAS Number1192-62-7

Synonymsmethyl furan-2-yl ketone; 2-acetyl-furan; 2-acetyl-fura; 2-ACETOFURONE; 2-Acetalfurnan; T5OJ BV1; EINECS 214-757-1; 1-(Furan-2-yl)ethanone; α-Methylfurfural; 2-Acetylfuran; 2-furylmethyl; 1-(Furan-2-yl)ethan-1-one; 1-(2-Furanyl)ethanone; 2-Furyl methyl ketone; ACF; FEMA 3163; furan-2-yl methyl ketone; Ketone, 2-furyl methyl; 1-(2-Furyl)ethanone; 2-furyl; MFCD00003242; 2-furfuryl methyl ketone; ACETYLFURAN; Methyl 2-furyl ketone; 1-(2-Furyl)ethan-1-one; 2-ACETYL FURAN

Molecular FormulaC6H6O2

Molecular Weight110.11

Purity99%

Density1.1±0.1 g/cm3

Boiling Point67 °C/10 mmHg (lit.)

Melting Point26-28 °C (lit.)

Flash Point

Appearanceliquid

EINECS214-757-1

MSDSChineseEnglish

Symbol6.1

Signal WordWarning

Cat. No.: 2A-9002216 Purity: 99%
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Quality Control of [ 1192-62-7 ] Purity: 99% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number1192-62-7
Catalog No.2A-9002216
Chinese Name2-乙酰基呋喃
Synonymsmethyl furan-2-yl ketone; 2-acetyl-furan; 2-acetyl-fura; 2-ACETOFURONE; 2-Acetalfurnan; T5OJ BV1; EINECS 214-757-1; 1-(Furan-2-yl)ethanone; α-Methylfurfural; 2-Acetylfuran; 2-furylmethyl; 1-(Furan-2-yl)ethan-1-one; 1-(2-Furanyl)ethanone; 2-Furyl methyl ketone; ACF; FEMA 3163; furan-2-yl methyl ketone; Ketone, 2-furyl methyl; 1-(2-Furyl)ethanone; 2-furyl; MFCD00003242; 2-furfuryl methyl ketone; ACETYLFURAN; Methyl 2-furyl ketone; 1-(2-Furyl)ethan-1-one; 2-ACETYL FURAN
Molecular FormulaC6H6O2
Molecular Weight110.11
Purity99
Density1.1±0.1 g/cm3
Boiling Point67 °C/10 mmHg (lit.)
Melting Point26-28 °C (lit.)
Appearanceliquid
Water SolubilityWater solubility: insoluble; soluble in: methanol
Storage ConditionSeal and store at 4 ºC
PackagingII
Application2-Acetylfuran (2-Furyl methyl ketone) is an important flavor compound or food intermediate that can be isolated from essential oils, sweet corn products, fruits and flowers. 2-Acetylfuran can also be
EINECS214-757-1
HTC2932190090
UN(IATA)UN 2811
PubChem ID24890568
MDL NumberMFCD00003242
SMILESCC(=O)c1ccco1
InChI1S/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H3
InChI KeyIEMMBWWQXVXBEU-UHFFFAOYSA-N
Beilstein/REAXYS107909
NACRES CodeNA.22
UNSPSC12352100
Hazard Symbols6.1
Risk CodesR23/25;R36/37
Safety DescriptionS26;S28A;S38;S39;S45
MSDSmsds/2216_1_1192_62_7.pdf
Bioactivity2-Acetylfuran (2-Furyl methyl ketone), an important flavour compound or intermediate in foods, is isolated from essential oils, sweet corn products, fruits and flowers. 2-Acetylfuran also can be formed from glucose and glycine by Maillard reaction. 2-Acetylfuran can be used to synthesis Cefuroxime[1][2]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Wang Y, et al. Amino acid-dependent formation pathways of 2-acetylfuran and 2,5-dimethyl-4-hydroxy-3[2H]-furanone in the Maillard reaction. Food Chemistry. 2009 Jul 1; 115(1):233-237. [2]. Banerjee R, et, al. Medicinal significance of furan derivatives: A Review . International Journal of Research in Phytochemistry and Pharmacology. 2015, 5(3):48-57. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 183.4±0.0 °C at 760 mmHg Melting Point 26-28 °C(lit.) Molecular Formula C6H6O2 Molecular Weight 110.111 Flash Point 71.1±0.0 °C Exact Mass 110.036781 PSA 30.21000 LogP 0.52 Vapour Pressure 0.8±0.3 mmHg at 25°C Index of Refraction 1.463 InChIKey IEMMBWWQXVXBEU-UHFFFAOYSA-N SMILES CC(=O)c1ccco1
Use of2-Acetylfuran (2-Furyl methyl ketone), an important flavour compound or intermediate in foods, is isolated from essential oils, sweet corn products, fruits and flowers. 2-Acetylfuran also can be formed from glucose and glycine by Maillard reaction. 2-Acetylfuran can be used to synthesis Cefuroxime[1][2]. Properties Name 2-acetylfuran Synonym More Synonyms 1-(Furan-2-yl)ethanone Biological Activity Description 2-Acetylfuran (2-Furyl methyl ketone), an important flavour compound or intermediate in foods, is isolated from essential oils, sweet corn products, fruits and flowers. 2-Acetylfuran also can be formed from glucose and glycine by Maillard reaction. 2-Acetylfuran can be used to synthesis Cefuroxime[1][2]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Wang Y, et al. Amino acid-dependent formation pathways of 2-acetylfuran and 2,5-dimethyl-4-hydroxy-3[2H]-furanone in the Maillard reaction. Food Chemistry. 2009 Jul 1; 115(1):233-237. [2]. Banerjee R, et, al. Medicinal significance of furan derivatives: A Review . International Journal of Research in Phytochemistry and Pharmacology. 2015, 5(3):48-57. Chemical & Physical Properties Molecular Formula C6H6O2 Exact Mass 110.036781 PSA 30.21000 Index of Refraction 1.463 InChIKey IEMMBWWQXVXBEU-UHFFFAOYSA-N
Tax Rebate9.0%
SupervisionNone MFN tariff: 6.5% Ordinary tariff: 20.0%
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Dangerous Regulations for land transport: 2811 International Dangerous Regulations for sea transport: 2811 International Dangerous Regulations for air transport: 2811 14.2 United Nations shipping name European Land Transport Dangerous Regulations: TOXIC SOLID, ORGANIC, N.O.S. (2-Furyl methyl ketone) IMDG: TOXIC SOLID, ORGANIC, N.O.S. (2-Furyl methyl ketone) International air transport hazard regulations: Toxic solid, organic, n.o.s. (2-Furyl methyl ketone) 14.3 Transport hazard categories European Land Transport Danger Regulations: 6.1 International Maritime Transport Danger Regulations: 6.1 International Air Transport Danger Regulations: 6.1 14.4 Package group European Dangerous Regulations for land transport: II International Dangerous Regulations for sea transport: II International Dangerous Regulations for air transport: II 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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