추천 제품
Grade
technical grade
Quality Level
분석
90%
refractive index
n20/D 1.468 (lit.)
bp
200 °C (lit.)
density
0.982 g/mL at 25 °C (lit.)
작용기
ether
ketone
저장 온도
2-8°C
SMILES string
[H]\C(OC)=C(\[H])C(C)=O
InChI
1S/C5H8O2/c1-5(6)3-4-7-2/h3-4H,1-2H3/b4-3+
InChI key
VLLHEPHWWIDUSS-ONEGZZNKSA-N
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일반 설명
trans-4-Methoxy-3-buten-2-one acts as substrate and undergoes zinc triflate-catalyzed Mukaiyama-Michael reaction with 3-TBSO-substituted vinyldiazoacetate to yield functionalized 3-keto-2-diazoalkanoates.
애플리케이션
trans-4-Methoxy-3-buten-2-one was used as starting reagent for enantioselective total synthesis of (-)-epibatidine.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
145.4 °F - closed cup
Flash Point (°C)
63 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Bifunctional thiourea-catalyzed enantioselective double Michael reaction of ?, d-unsaturated ?-ketoester to nitroalkene: asymmetric synthesis of (-)-epibatidine.
Tetrahedron Letters, 45(50), 9185-9188 (2004)
Organic letters, 12(19), 4304-4307 (2010-09-03)
Enedione-diazoesters formed from 3-TBSO-2-diazo-3-butenoates undergo base-catalyzed pericyclization that with dinitrogen extrusion and methyl migration provide a novel and efficient route to 2-carboalkoxyresorcinols. Intercepting the intermediate enolate anion with methyl vinyl ketone leads to the corresponding 4-substituted 2-carboalkoxyresorcinol and suggests generalization
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