CAS 1192-62-7|1-(Furan-2-yl)ethanone

Introduction：Basic information about CAS 1192-62-7|1-(Furan-2-yl)ethanone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. 1-(Furan-2-yl)ethanone BiologicalActivity
3. Chemical & Physical Properties
4. Toxicological Information
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
MUTATION DATA
5. Safety Information
6. Customs
7. Articles9
8. Synonyms

Common Name	1-(Furan-2-yl)ethanone
CAS Number	1192-62-7	Molecular Weight	110.111
Density	1.1±0.1 g/cm3	Boiling Point	183.4±0.0 °C at 760 mmHg
Molecular Formula	C₆H₆O₂	Melting Point	26-28 °C(lit.)
MSDS	ChineseUSA	Flash Point	71.1±0.0 °C
Symbol	GHS05, GHS06	Signal Word	Danger

Names

Name	2-acetylfuran
Synonym	More Synonyms

1-(Furan-2-yl)ethanone BiologicalActivity

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 >>OthersSignaling 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.

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 >>OthersSignaling 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

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: OB3870000

CHEMICAL NAME :: Ketone, 2-furyl methyl

CAS REGISTRY NUMBER :: 1192-62-7

BEILSTEIN REFERENCE NO. :: 0107909

LAST UPDATED :: 199710

DATA ITEMS CITED :: 5

MOLECULAR FORMULA :: C6-H6-O2

MOLECULAR WEIGHT :: 110.12

WISWESSER LINE NOTATION :: T5OJ BV1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: Cytogenetic analysis

TEST SYSTEM :: Rodent - hamster Ovary

DOSE/DURATION :: 4500 umol/L

REFERENCE :: CALEDQ Cancer Letters (Shannon, Ireland). (Elsevier Scientific Pub. Ireland Ltd., POB 85, Limerick, Ireland) V.1- 1975- Volume(issue)/page/year: 13,89,1981

Safety Information

Symbol	GHS05, GHS06
Signal Word	Danger
Hazard Statements	H300-H311-H318-H332
Precautionary Statements	P264-P280-P301 + P310-P305 + P351 + P338-P312
Personal Protective Equipment	Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges
Hazard Codes	T:Toxic
Risk Phrases	R23/25;R36/37
Safety Phrases	S26-S36/37/39-S45-S39-S38-S28A
RIDADR	UN 2811 6.1/PG 2
WGK Germany	3
RTECS	OB3870000
Packaging Group	II
Hazard Class	6.1
HS Code	2932190090

Customs

HS Code	2932190090
Summary	2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles9

Quantification of furanic derivatives in fortified wines by a highly sensitive and ultrafast analytical strategy based on digitally controlled microextraction by packed sorbent combined with ultrahigh pressure liquid chromatography.

J. Chromatogr. A. 1381 , 54-63, (2015)

An improved, reliable and powerful analytical strategy based on digitally controlled microextraction by packed sorbent (MEPS) combined with ultrahigh pressure liquid chromatography (UHPLC) was validat...

Dose-dependent increase in 2,5-hexanedione in the urine of workers exposed to n-hexane.

Int. Arch. Occup. Environ. Health 63(4) , 285-91, (1991)

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 an...

2-Acetylfuran, a confounder in urinalysis for 2,5-hexanedione as an n-hexane exposure indicator.

Int. Arch. Occup. Environ. Health 63(3) , 213-9, (1991)

The apparent amount of 2,5-hexanedione, a biomarker of n-hexane expsoure in occupational health, in the urine of both exposed and non-exposed subjects varied not only as a function of the pH at which ...

Synonyms

methyl 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

Furan, 2-acetyl-

Ethanone, 1- (2-furanyl)-

ACF

FEMA 3163

Ethanone, 1-(2-furanyl)-

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

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