D183407
2,6-Dimethyl-γ-pyrone
99%
Synonym(s):
2,6-Dimethyl-4H-pyran-4-one
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About This Item
Empirical Formula (Hill Notation):
C7H8O2
CAS Number:
Molecular Weight:
124.14
Beilstein:
107418
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
solid
bp
248-250 °C (lit.)
mp
133-137 °C (lit.)
SMILES string
CC1=CC(=O)C=C(C)O1
InChI
1S/C7H8O2/c1-5-3-7(8)4-6(2)9-5/h3-4H,1-2H3
InChI key
VSYFZULSKMFUJJ-UHFFFAOYSA-N
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Related Categories
Application
2,6-Dimethyl-γ-pyrone can be used as a starting material to prepare:
- C16-C28 spiroketal fragment of altohyrtin A.
- 1-Ethyl-2,6-dimethyl-4-hydroxy pyridinium halides.
- 2-{2,6-Bis-[2-(4-dimethylamino-phenyl)-vinyl]-pyran-4-ylidene}-malononitrile, applicable in two-photon technology.
- Pyran-derived polyurethanes for nonlinear optical (NLO) applications.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis, structural, thermal and optical studies of 1-ethyl-2, 6-dimethyl-4-hydroxy pyridinium halides
Dhanuskodi S, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 64(2), 504-511 (2006)
Synthesis of the C16-C28 Spiroketal Subunit of Spongistatin 1 (Altohyrtin A): The Pyrone Approach
Crimmins MT and Katz JD
Organic Letters, 2(7), 957-960 (2000)
Synthesis and second-harmonic generation study of DCM-containing polyurethane
Yoon C-B, et al.
Synthetic Metals, 117(1-3), 233-235 (2001)
Two-photon absorption properties of malononitrile derivatives
Zhao Y, et al.
Optical Materials, 29(9), 1206-1210 (2007)
Karen A Nolan et al.
Bioorganic & medicinal chemistry letters, 16(24), 6246-6254 (2006-10-03)
From in silico docking and COMPARE analysis, novel inhibitors of human NAD(P)H quinone oxidoreductase (NQO1) have been identified from the NCI compound database, the most potent of which has an observed IC(50) of 0.7muM. The inhibitors exhibit a diverse range
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