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Merck

370207

Sigma-Aldrich

4,6-Dimethyl-α-pyrone

98%

Sinónimos:

4,6-Dimethyl-2H-pyran-2-one

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About This Item

Fórmula empírica (notación de Hill):
C7H8O2
Número de CAS:
Peso molecular:
124.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

48-50 °C (lit.)

SMILES string

CC1=CC(C)=CC(=O)O1

InChI

1S/C7H8O2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3

InChI key

IXYLIUKQQQXXON-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

General description

4,6-Dimethyl-α-pyrone was immobilized in a guanidinium-sulfonate-calixarene (G4C) crystalline network, which upon exposure to ultraviolet irradiation, transforms the entrapped 4,6-dimethyl-α-pyrone into a 4,6-dimethyl-β-lactone. Thin solid films layers of 4,6-dimethyl-α-pyrone on UV irradiation at -190°C were investigated.

Application

4,6-Dimethyl-α-pyrone (Me21) has been used in the preparation of G4C{Me21} via reacting with tetra-p-sulfocalix[4]arene (C) and guanidine hydrochloride (GCl). It may be used in the preparation of host-guest complex G4C{Me21} by reacting with crystalline guanidinium-sulfonate-calixarene (G4C). This complex on UV irradiation afforded 1,3-dimethylcyclobutadiene (Me2CBD).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Yves-Marie Legrand et al.
Science (New York, N.Y.), 329(5989), 299-302 (2010-07-22)
Cyclobutadiene (CBD), the smallest cyclic hydrocarbon bearing conjugated double bonds, has long intrigued chemists on account of its strained geometry and electronic instability, but the parent compound and its unperturbed derivatives have thus far eluded crystallographic characterization. In this work
4, 6-Dimethyl-a-pyrone: a matrix isolation study of the photochemical generation of conjugated ketene, Dewar valence isomer and 1, 3-dimethyl-cyclobutadiene.
Breda S, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 162(1), 139-151 (2004)
Yves-Marie Legrand et al.
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Cyclobutadiene (CBD), the smallest cyclic hydrocarbon bearing conjugated double bonds, has long intrigued chemists because of its chemical characteristics. The question of whether the molecule could be prepared at all has been answered, but the parent compound and its unperturbed

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