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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
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.
1989 Mar 5
Formation of Amadori compounds in dehydrated fruits.
2001 Nov
Antituberculosis agents. VI. Activity of a new ciprofloxacin derivative against Mycobacterium avium and some drug-resistant strains of Mycobacterium tuberculosis.
2002 Sep-Oct
Determination of furanic compounds in traditional balsamic vinegars by ion-exclusion liquid chromatography and diode-array detection.
2003 Jul
2-Furoylmethyl amino acids and hydroxymethylfurfural as indicators of honey quality.
2003 Jul 16
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.
2003 May 21
Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents.
2004 Jul 1
Analysis of potential and free furfural compounds in milk-based formulae by high-performance liquid chromatography. Evolution during storage.
2005 May 27
Synthesis and antiamoebic activity of new oxime ether derivatives containing 2-acetylpyridine/2-acetylfuran.
2005 Oct 1
Synthesis, characterization, and biotoxicity of N N donor sulphonamide imine silicon(IV) complexes.
2006
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 Jan 24
Characterization of a new Maillard type reaction product generated by heating 1-deoxymaltulosyl-glycine in the presence of cysteine.
2006 Jul 12
Elemental sulfur identified in urine of cheetah, Acinonyx jubatus.
2006 Jun
Asymmetric synthesis of methyl 6-deoxy-3-O-methyl-alpha-L-mannopyranoside from a non-carbohydrate precursor.
2006 May 1
Spectral studies on Co(II), Ni(II) and Cu(II) complexes with thiosemicarbazone (L1) and semicarbazone (L2) derived from 2-acetyl furan.
2007 Apr
Spectroscopic evaluation of Co(II), Ni(II) and Cu(II) complexes derived from thiosemicarbazone and semicarbazone.
2007 Dec 31
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
2007 Jan 24
Comparison of 2-acetylfuran formation between ribose and glucose in the Maillard reaction.
2008 Dec 24
Monitoring cytotoxic potentials of furfuryl alcohol and 2-furyl methyl ketone in mice.
2008 Jan
N'-[1-(2-Fur-yl)ethen-yl]propanohydrazide.
2008 Jan 23
(E)-3-(2-Chloro-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008 Jul 12
De novo asymmetric synthesis of anthrax tetrasaccharide and related tetrasaccharide.
2008 Jul 18
(E)-3-(4-Chloro-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008 Jul 19
3-Ethyl-4-[(E)-2-methyl-benzyl-idene-amino]-1H-1,2,4-triazole-5(4H)-thione.
2008 Jul 5
2-Methyl-benzaldehyde 2-methyl-benzyl-idenehydrazone.
2008 Jul 5
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.
2008 Jul 9
(E)-2-Acetyl-pyrazine 4-nitro-phenyl-hydrazone.
2008 Jun 13
3-Penta-none 2,4-dinitro-phenyl-hydrazone.
2008 Jun 7
(E)-2-Furyl methyl ketone 2,4-dinitro-phenyl-hydrazone.
2008 May 24
1,2-Bis(2-furylmethyl-ene)hydrazine.
2008 Sep 27
A circuit supporting concentration-invariant odor perception in Drosophila.
2009
Investigation of trypanothione reductase as a drug target in Trypanosoma brucei.
2009 Dec
3-(2,4-Dichloro-phen-yl)-1,5-di-2-furylpentane-1,5-dione.
2009 Jan 17
Identification of hydroxycinnamic acid-maillard reaction products in low-moisture baking model systems.
2009 Nov 11
Highly enantioselective 3-furylation of ketones using (3-furyl)titanium nucleophile.
2010 Jan 1
Simple and convenient approach to the Kreohnke pyridine type synthesis of functionalized indol-3-yl pyridine derivatives using 3-cyanoacetyl indole.
2010 Jan-Feb
(E)-1-(2-Fur-yl)-3-(3,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010 Nov 6
(E)-1-(2-Fur-yl)-3-(2,4,6-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010 Sep 15
Wound contraction effects and antibacterial properties of Tualang honey on full-thickness burn wounds in rats in comparison to hydrofibre.
2010 Sep 3
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:37:33 GMT 2023
Edited
by admin
on Fri Dec 15 17:37:33 GMT 2023
Record UNII
Q5ZRP80K02
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-ACETYLFURAN
FHFI  
Systematic Name English
2-FURYL METHYL KETONE
FCC  
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 Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
Code System Code Type Description
NSC
4665
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
CHEBI
59983
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-757-1
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
WIKIPEDIA
2-Acetylfuran
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
MESH
C039669
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
CAS
1192-62-7
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
JECFA MONOGRAPH
1494
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
NSC
49133
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
FDA UNII
Q5ZRP80K02
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
PUBCHEM
14505
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID0051601
Created by admin on Fri Dec 15 17:37:33 GMT 2023 , Edited by admin on Fri Dec 15 17:37:33 GMT 2023
PRIMARY