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经验公式(希尔记法):
C7H8O2
化学文摘社编号:
分子量:
124.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-719-1
Beilstein/REAXYS Number:
107418
MDL number:
产品名称
2,6-二甲基-γ-吡喃酮, 99%
InChI key
VSYFZULSKMFUJJ-UHFFFAOYSA-N
InChI
1S/C7H8O2/c1-5-3-7(8)4-6(2)9-5/h3-4H,1-2H3
SMILES string
CC1=CC(=O)C=C(C)O1
assay
99%
form
solid
bp
248-250 °C (lit.)
mp
133-137 °C (lit.)
Quality Level
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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.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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