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About This Item
线性分子式:
(C2H5O)2CHCH=C(CH3)2
CAS号:
分子量:
158.24
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
97%
折射率
n20/D 1.421 (lit.)
bp
53-58 °C/20 mmHg (lit.)
密度
0.837 g/mL at 25 °C (lit.)
SMILES字符串
CCOC(OCC)\C=C(\C)C
InChI
1S/C9H18O2/c1-5-10-9(11-6-2)7-8(3)4/h7,9H,5-6H2,1-4H3
InChI key
SFUKGEREDDIOED-UHFFFAOYSA-N
一般描述
1,1-Diethoxy-3-methyl-2-butene is an acyclic alkene.
应用
1,1-Diethoxy-3-methyl-2-butene may be used in the synthesis of:
- 6,6,10-trimethyl-4-propyl-10,11-dihydro-2H,6H,12H-dipyrano[2,3-f:2′,3′-h]chromene-2,12-dione
- angular pyranocoumarins
- 6-cyano-2,2-dimethyl-2-H-1-benzopyran
Tao Ma et al.
Journal of medicinal chemistry, 51(5), 1432-1446 (2008-02-21)
(+)-Calanolide A ( 1) as a natural product was previously found as an inhibitor of HIV-1 reverse transcriptase. In our further investigation of its template, racemic 11-demethyl-12-oxo calanolide A ( 15), which had two fewer chiral carbon centers at the
Convenient synthesis of linear pyrano [3, 2-g]-,[2, 3-g]-and angular pyrano [3, 2-f] coumarins from 4 [(1, 1-dimethyl-2-propynyl) oxy] phenol.
Baldoumi, V., et al.
Tetrahedron, 62(34), 8016-8020 (2006)
Green synthesis of 6-cyano-2, 2-dimethyl-2-H-1-benzopyran and its subsequent enantioselective epoxidation.
Romanelli G, et al.
J. Mol. Catal. A: Chem., 398, 11-16 (2015)
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