추천 제품
Quality Level
분석
96%
양식
liquid
refractive index
n20/D 1.398 (lit.)
bp
125 °C (lit.)
density
0.854 g/mL at 25 °C (lit.)
SMILES string
CCOC(OCC)C=C
InChI
1S/C7H14O2/c1-4-7(8-5-2)9-6-3/h4,7H,1,5-6H2,2-3H3
InChI key
MCIPQLOKVXSHTD-UHFFFAOYSA-N
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애플리케이션
Acrolein diethyl acetal is widely used to carry out chemoselective Heck arylation to synthesize either 3-arylpropanoate esters or cinnamaldehyde derivatives.
It can also be used as one of the precursors to synthesize natural products like (−)-(Z)-Deoxypukalide, (−)-Laulimalide, botryodiplodin, neolaulimalide and isolaulimalide.
It can also be used as one of the precursors to synthesize natural products like (−)-(Z)-Deoxypukalide, (−)-Laulimalide, botryodiplodin, neolaulimalide and isolaulimalide.
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
59.0 °F - closed cup
Flash Point (°C)
15 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis of (?)-and (−)-botryodiplodin using stereoselective radical cyclizations of acyclic esters and acetals.
Tetrahedron Asymmetry, 14(19), 3005-3018 (2003)
Total synthesis of neolaulimalide and isolaulimalide.
Organic Letters, 10(20), 4701-4704 (2008)
Chemoselective Heck arylation of acrolein diethyl acetal catalyzed by an oxime-derived palladacycle.
Tetrahedron, 61(41), 9688-9695 (2005)
Total Synthesis of Microtubule-Stabilizing Agent (-)-Laulimalide1.
The Journal of Organic Chemistry, 66(26), 8973-8982 (2001)
An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides.
Organic Letters, 5(5), 777-780 (2003)
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