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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6O2
Molecular Weight 110.1106
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-Acetylfuran

SMILES

CC(=O)C1=CC=CO1

InChI

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

HIDE SMILES / InChI

Molecular Formula C6H6O2
Molecular Weight 110.1106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(E)-1-(2-Fur-yl)-3-(3,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010-11-06
(E)-1-(2-Fur-yl)-3-(2,4,6-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010-09-15
Wound contraction effects and antibacterial properties of Tualang honey on full-thickness burn wounds in rats in comparison to hydrofibre.
2010-09-03
Highly enantioselective 3-furylation of ketones using (3-furyl)titanium nucleophile.
2010-01-01
Investigation of trypanothione reductase as a drug target in Trypanosoma brucei.
2009-12
Simple and convenient approach to the Kreohnke pyridine type synthesis of functionalized indol-3-yl pyridine derivatives using 3-cyanoacetyl indole.
2009-11-13
Identification of hydroxycinnamic acid-maillard reaction products in low-moisture baking model systems.
2009-11-11
3-(2,4-Dichloro-phen-yl)-1,5-di-2-furylpentane-1,5-dione.
2009-01-17
A circuit supporting concentration-invariant odor perception in Drosophila.
2009
Comparison of 2-acetylfuran formation between ribose and glucose in the Maillard reaction.
2008-12-24
1,2-Bis(2-furylmethyl-ene)hydrazine.
2008-09-27
(E)-3-(4-Chloro-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008-07-19
De novo asymmetric synthesis of anthrax tetrasaccharide and related tetrasaccharide.
2008-07-18
(E)-3-(2-Chloro-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008-07-12
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008-07-09
3-Ethyl-4-[(E)-2-methyl-benzyl-idene-amino]-1H-1,2,4-triazole-5(4H)-thione.
2008-07-05
2-Methyl-benzaldehyde 2-methyl-benzyl-idenehydrazone.
2008-07-05
(E)-2-Acetyl-pyrazine 4-nitro-phenyl-hydrazone.
2008-06-13
3-Penta-none 2,4-dinitro-phenyl-hydrazone.
2008-06-07
(E)-2-Furyl methyl ketone 2,4-dinitro-phenyl-hydrazone.
2008-05-24
N'-[1-(2-Fur-yl)ethen-yl]propanohydrazide.
2008-01-23
Monitoring cytotoxic potentials of furfuryl alcohol and 2-furyl methyl ketone in mice.
2008-01
Spectroscopic evaluation of Co(II), Ni(II) and Cu(II) complexes derived from thiosemicarbazone and semicarbazone.
2007-12-31
Spectral studies on Co(II), Ni(II) and Cu(II) complexes with thiosemicarbazone (L1) and semicarbazone (L2) derived from 2-acetyl furan.
2007-04
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
2007-01-24
Characterization of a new Maillard type reaction product generated by heating 1-deoxymaltulosyl-glycine in the presence of cysteine.
2006-07-12
Elemental sulfur identified in urine of cheetah, Acinonyx jubatus.
2006-06
Asymmetric synthesis of methyl 6-deoxy-3-O-methyl-alpha-L-mannopyranoside from a non-carbohydrate precursor.
2006-05-01
Purification and characterization of a furfural reductase (FFR) from Escherichia coli strain LYO1--an enzyme important in the detoxification of furfural during ethanol production.
2006-01-24
Synthesis, characterization, and biotoxicity of N N donor sulphonamide imine silicon(IV) complexes.
2006
Synthesis and antiamoebic activity of new oxime ether derivatives containing 2-acetylpyridine/2-acetylfuran.
2005-10-01
Analysis of potential and free furfural compounds in milk-based formulae by high-performance liquid chromatography. Evolution during storage.
2005-05-27
Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents.
2004-07-01
Characterization of odor-active compounds in Californian chardonnay wines using GC-olfactometry and GC-mass spectrometry.
2003-12-31
2-Furoylmethyl amino acids and hydroxymethylfurfural as indicators of honey quality.
2003-07-16
Determination of furanic compounds in traditional balsamic vinegars by ion-exclusion liquid chromatography and diode-array detection.
2003-07
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.
2003-05-21
Antituberculosis agents. VI. Activity of a new ciprofloxacin derivative against Mycobacterium avium and some drug-resistant strains of Mycobacterium tuberculosis.
2002-12-17
Formation of Amadori compounds in dehydrated fruits.
2001-11
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.
1989-03-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:49:40 GMT 2025
Edited
by admin
on Mon Mar 31 18:49:40 GMT 2025
Record UNII
Q5ZRP80K02
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-FURYL METHYL KETONE
FCC  
Preferred Name English
2-Acetylfuran
FHFI  
Systematic Name English
2-FURYL METHYL KETONE [FCC]
Common Name English
2-ACETYL FURAN
Systematic Name English
FEMA NO. 3163
Code English
2-ACETYLFURAN [FHFI]
Common Name English
ETHANONE, 1-(2-FURANYL)-
Systematic Name English
NSC-4665
Code English
NSC-49133
Code English
KETONE, 2-FURYL METHYL
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2-FURYL METHYL KETONE
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
Code System Code Type Description
NSC
4665
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
CHEBI
59983
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-757-1
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
WIKIPEDIA
2-Acetylfuran
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
MESH
C039669
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
CAS
1192-62-7
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
JECFA MONOGRAPH
1494
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
NSC
49133
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
FDA UNII
Q5ZRP80K02
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
PUBCHEM
14505
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID0051601
Created by admin on Mon Mar 31 18:49:40 GMT 2025 , Edited by admin on Mon Mar 31 18:49:40 GMT 2025
PRIMARY