2-ACETYLFURAN

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 Search

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

Title	Date	PubMed
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.	1989 Mar 5	2917974
Antituberculosis agents. VI. Activity of a new ciprofloxacin derivative against Mycobacterium avium and some drug-resistant strains of Mycobacterium tuberculosis.	2002 Sep-Oct	12481384
Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents.	2004 Jul 1	15214792
Analysis of potential and free furfural compounds in milk-based formulae by high-performance liquid chromatography. Evolution during storage.	2005 May 27	15974079
Synthesis, characterization, and biotoxicity of N N donor sulphonamide imine silicon(IV) complexes.	2006	17496998
Characterization of a new Maillard type reaction product generated by heating 1-deoxymaltulosyl-glycine in the presence of cysteine.	2006 Jul 12	16819926
Spectral studies on Co(II), Ni(II) and Cu(II) complexes with thiosemicarbazone (L1) and semicarbazone (L2) derived from 2-acetyl furan.	2007 Apr	16919999
Spectroscopic evaluation of Co(II), Ni(II) and Cu(II) complexes derived from thiosemicarbazone and semicarbazone.	2007 Dec 31	17418625
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.	2007 Jan 24	17227073
Comparison of 2-acetylfuran formation between ribose and glucose in the Maillard reaction.	2008 Dec 24	19090713
Monitoring cytotoxic potentials of furfuryl alcohol and 2-furyl methyl ketone in mice.	2008 Jan	17904264
De novo asymmetric synthesis of anthrax tetrasaccharide and related tetrasaccharide.	2008 Jul 18	18563936
3-Ethyl-4-[(E)-2-methyl-benzyl-idene-amino]-1H-1,2,4-triazole-5(4H)-thione.	2008 Jul 5	21203120
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-fur-yl)prop-2-en-1-one.	2008 Jul 9	21203150
(E)-2-Furyl methyl ketone 2,4-dinitro-phenyl-hydrazone.	2008 May 24	21202661
1,2-Bis(2-furylmethyl-ene)hydrazine.	2008 Sep 27	21201220
A circuit supporting concentration-invariant odor perception in Drosophila.	2009	19171076
Investigation of trypanothione reductase as a drug target in Trypanosoma brucei.	2009 Dec	19924760
Identification of hydroxycinnamic acid-maillard reaction products in low-moisture baking model systems.	2009 Nov 11	19817410
Highly enantioselective 3-furylation of ketones using (3-furyl)titanium nucleophile.	2010 Jan 1	19958037
Simple and convenient approach to the Kreohnke pyridine type synthesis of functionalized indol-3-yl pyridine derivatives using 3-cyanoacetyl indole.	2010 Jan-Feb	19905001
(E)-1-(2-Fur-yl)-3-(3,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.	2010 Nov 6	21589380
(E)-1-(2-Fur-yl)-3-(2,4,6-trimeth-oxy-phen-yl)prop-2-en-1-one.	2010 Sep 15	21587546

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

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Name

Type

Language

2-ACETYLFURAN

Systematic Name

English

2-FURYL METHYL KETONE

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