190543
丙烯醛二甲缩醛
98%
别名:
3,3-二甲氧基-1-丙烯
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线性分子式:
H2C=CHCH(OCH3)2
化学文摘社编号:
分子量:
102.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-936-4
Beilstein/REAXYS Number:
1700037
MDL number:
产品名称
丙烯醛二甲缩醛, 98%
InChI key
OBWGMYALGNDUNM-UHFFFAOYSA-N
InChI
1S/C5H10O2/c1-4-5(6-2)7-3/h4-5H,1H2,2-3H3
SMILES string
COC(OC)C=C
assay
98%
form
liquid
refractive index
n20/D 1.395 (lit.)
bp
89-90 °C (lit.)
density
0.862 g/mL at 25 °C (lit.)
functional group
acetal
ether
Quality Level
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Application
Acrolein dimethyl acetal was used in the facile one step synthesis of 4-hydroxy-2E-nonenal and its dimethyl acetal via a cross-metathesis reaction with octen-3-ol.
General description
Acrolein dimethyl acetal undergoes cationic α-diimine palladium chelate catalyzed copolymerization with ethene to yield branched copolymers.
Weidong Li et al.
Journal of the American Chemical Society, 126(39), 12246-12247 (2004-09-30)
Acrolein dimethyl acetal (ADMA) can be copolymerized with ethene using a cationic alpha-diimine palladium chelate catalyst to yield branched copolymers. Catalyst deactivation occurs via methanol elimination to give an inert eta3-1-methoxyallyl palladium species. This process can be retarded by the
Laurent Soulère et al.
Chemistry and physics of lipids, 150(2), 239-243 (2007-10-05)
The facile one step synthesis of 4-hydroxy-2E-nonenal and its dimethyl acetal via a cross-metathesis reaction between commercially available octen-3-ol and acrolein or its dimethyl acetal is reported. The method was extended to the synthesis of C6 and C12 4-hydroxy-2E-enals, their
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