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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 5-METHYL-2-FURALDEHYDE

SMILES

CC1=CC=C(O1)C=O

InChI

InChIKey=OUDFNZMQXZILJD-UHFFFAOYSA-N
InChI=1S/C6H6O2/c1-5-2-3-6(4-7)8-5/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
A new method for the determination of carbonyl compounds in wines by headspace solid-phase microextraction coupled to gas chromatography-ion trap mass spectrometry.
2010-12-22
Biodetoxification of toxins generated from lignocellulose pretreatment using a newly isolated fungus, Amorphotheca resinae ZN1, and the consequent ethanol fermentation.
2010-11-22
Wound contraction effects and antibacterial properties of Tualang honey on full-thickness burn wounds in rats in comparison to hydrofibre.
2010-09-03
4-{2-[(Z)-(5-Methyl-2-fur-yl)methyl-idene-amino]-eth-yl}benzene-sulfonamide.
2010-08-28
Essential oil of Terminalia chebula fruits as a repellent for the indian honeybee Apis florea.
2010-05
N'-[(5-Methyl-2-fur-yl)methyl-ene]thio-phene-2-carbohydrazide.
2010-03-27
Coffee aroma--statistical analysis of compositional data.
2009-12-15
Hydrothermal processing and enzymatic hydrolysis of sorghum bagasse for fermentable carbohydrates production.
2009-12
1-(4-Chloro-phen-yl)-3-(5-methyl-2-fur-yl)prop-2-en-1-one.
2009-10-31
3-Hydr-oxy-N'-[(Z)-(5-methyl-2-fur-yl)methyl-idene]naphthalene-2-carbo-hydrazide.
2009-10-23
Catalytic pyrolysis of cellulose with sulfated metal oxides: a promising method for obtaining high yield of light furan compounds.
2009-10
N'-[(E)-(5-Methyl-furan-2-yl)methyl-idene]formohydrazide.
2009-09-19
3-[(5-Methyl-furan-2-yl)methyl-ene]-1,5-dioxaspiro-[5.5]undecane-2,4-dione.
2009-07-29
Simple gas chromatographic method for furfural analysis.
2009-04-03
(E)-N-[(5-Methyl-2-fur-yl)methyl-ene]-3-nitro-aniline.
2009-03-06
Prediction of sensory properties of Brazilian Arabica roasted coffees by headspace solid phase microextraction-gas chromatography and partial least squares.
2009-02-23
Impact of forced-aging process on madeira wine flavor.
2008-12-24
N'-[(5-Methyl-furan-2-yl)methyl-ene]isonicotinohydrazide.
2008-11-20
Removal of phytotoxic compounds from torrefied grass fibres by plant-beneficial microorganisms.
2008-10
3-(5-Methyl-2-fur-yl)-1-(p-tol-yl)-2-propen-1-one.
2008-09-17
Importance of chip selection and elaboration process on the aromatic composition of finished wines.
2008-07-09
1,5-Dimethyl-4-[(5-methyl-2-furyl)-methyl-ene-amino]-2-phenyl-1H-pyrazol-3(2H)-one.
2008-05-30
Liquid alkanes with targeted molecular weights from biomass-derived carbohydrates.
2008
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.
2007-01-24
Influence of the species and geographical location on volatile composition of Spanish oak wood (Quercus petraea Liebl. and Quercus robur L.).
2006-04-19
Analysis of potential and free furfural compounds in milk-based formulae by high-performance liquid chromatography. Evolution during storage.
2005-05-27
3-Hydroxy-4,5-dimethyl-2(5H)-furanone levels in fortified Madeira wines: relationship to sugar content.
2004-11-03
Off-vine grape drying effect on volatile compounds and aromatic series in must from Pedro Ximénez grape variety.
2004-06-16
Influence of distillation system, oak wood type, and aging time on composition of cider brandy in phenolic and furanic compounds.
2003-12-31
Quantitative analysis of 2-furfural and 5-methylfurfural in different Italian vinegars by headspace solid-phase microextraction coupled to gas chromatography-mass spectrometry using isotope dilution.
2003-10-31
Application of solid-phase extraction for determination of phenolic compounds in barrique wines.
2003-09
Extraction and formation dynamic of oak-related volatile compounds from different volume barrels to wine and their behavior during bottle storage.
2003-08-27
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.
2003-05-21
Reaction of 1,4-phthalazinedione with furfural: formation of the [5,6]benza-3a,7a-diazaindane system via an unusual skeletal rearrangement.
2002-03-07
High-performance liquid chromatographic determination of furfural compounds in infant formulas. Changes during heat treatment and storage.
2002-02-15
Phytotoxic and fungitoxic activities of the essential oil of kenaf (Hibiscus cannabinus L.) leaves and its composition.
2001-08
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:12 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:12 GMT 2025
Record UNII
4482BZC72D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-METHYL FURFURAL
FCC   FHFI  
Preferred Name English
5-METHYL-2-FURALDEHYDE
Systematic Name English
5-METHYL FURFURAL [FCC]
Common Name English
5-METHYL-2-FURANCARBOXALDEHYDE
Systematic Name English
FEMA NO. 2702
Code English
5-METHYLFURAN-2-ALDEHYDE
Systematic Name English
2-FORMYL-5-METHYLTETRAHYDROFURAN
Systematic Name English
2-METHYL-5-FORMYLFURAN
Systematic Name English
2-FURANCARBOXALDEHYDE, 5-METHYL-
Systematic Name English
METHYL FURFURAL, 5-
Common Name English
5-METHYL-2-FURFURYLALDEHYDE
Common Name English
5-METHYLFURAN-2-AL
Systematic Name English
5-METHYLFURFURALDEHYDE
Systematic Name English
5-METHYL FURFURAL [FHFI]
Common Name English
5-METHYLFURAN-2-CARBALDEHYDE
Systematic Name English
METHYL-5-FURALDEHYDE
Systematic Name English
5-METHYL-2-FURFURAL
Common Name English
2-FORMYL-5-METHYLFURAN
Systematic Name English
5-METHYL-2-FURFURALDEHYDE
Common Name English
2-FURALDEHYDE, 5-METHYL-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 5-METHYLFURFURAL
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
Code System Code Type Description
EVMPD
SUB179498
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
SMS_ID
100000164905
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
CAS
620-02-0
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-622-6
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID1060714
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
FDA UNII
4482BZC72D
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
MESH
C048065
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
PUBCHEM
12097
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY
JECFA MONOGRAPH
1124
Created by admin on Mon Mar 31 18:51:12 GMT 2025 , Edited by admin on Mon Mar 31 18:51:12 GMT 2025
PRIMARY