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Merck

393509

Sigma-Aldrich

3-Methyl-2(5H)-furanone

technical grade, 90%

Sinónimos:

α-Methyl-γ-crotonolactone, 2-Methyl-2-butenolide, 2-Methylbut-2-en-4-olide, 3-Methyl-2,5-dihydrofuran-2-one, 3-Methyl-5H-furan-2-one, 4-Hydroxy-2-methyl-2-butenoic acid γ-lactone

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About This Item

Fórmula empírica (notación de Hill):
C5H6O2
Número de CAS:
Peso molecular:
98.10
Beilstein/REAXYS Number:
1642
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

assay

90%

form

liquid

refractive index

n20/D 1.467 (lit.)

bp

97-99 °C/20 mmHg (lit.)

density

1.13 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CC1=CCOC1=O

InChI

1S/C5H6O2/c1-4-2-3-7-5(4)6/h2H,3H2,1H3

InChI key

VGHBEMPMIVEGJP-UHFFFAOYSA-N

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General description

3-Methyl-2(5H)-furanone (3-Methylfuran-2(5H)-one) has been synthesized in highest yield (77%) by employing α-methyl-γ- butyrolactone as starting reagent.
3-Methyl-2(5H)-furanone, a five membered conjugated lactone, is a volatile compound. Its synthesis has been reported. It is reported to be one of the predominant constituent of the flavor of pandan leaves. It is also found in Thai soy sauce, Arabica roasted coffee samples from Brazil, bio-oil from pine wood sawdust.

Application

3-Methyl-2(5H)-furanone is the suitable model compound used to investigate the fragmentation mechanism of five membered lactones by electrospray ionisation tandem mass spectrometry and also to study the airway irritation of isoprene, isoprene/ozone, and isoprene/ozone/nitrogen dioxide mixture.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

200.1 °F - closed cup

flash_point_c

93.4 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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The fragmentation mechanism of five-membered lactones by electrospray ionisation tandem mass spectrometry.
Crotti AEM, et al.
International Journal of Mass Spectrometry, 232(3), 271-276 (2004)
Mengcen Wang et al.
PloS one, 8(11), e78024-e78024 (2013-11-14)
The tropolone-tolerant Trichoderma virens PS1-7 is a biocontrol agent against Burkholderia plantarii, causative of rice seedling blight. When exposed to catechol, this fungus dose-dependently produced carot-4-en-9,10-diol, a sesquiterpene-type autoregulatory signal molecule that promotes self-conidiation of T. virens PS1-7 mycelia. It
A New Expedient Synthesis of 3-Methyl-2 (5H)-furanone, the Common Substructure in Strigolactones, and Its Proposed Biosynthesis.
Malik H, et al.
Synthesis, 19, 3271-3273 (2010)
An efficient and short synthesis of 3-methyl-2 (5H)-furanone, a synthon for strigol analogues.
Mangnus EM and Zwanenburg B
Synthetic Communications, 22(5), 783-786 (1992)
A Useful Synthesis of 3-Methyl-2 (5H)-Furanone.
Cruz-Almanza R and Padilla Higareda F.
Synthetic Communications, 21(8-9), 1097-1104 (1991)

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