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方案
97%
反应适用性
reaction type: C-C Bond Formation
mp
120-122 °C (lit.)
官能团
ester
phenyl
phosphine
SMILES字符串
O=C(OCc1ccccc1)C=P(c2ccccc2)(c3ccccc3)c4ccccc4
InChI
1S/C27H23O2P/c28-27(29-21-23-13-5-1-6-14-23)22-30(24-15-7-2-8-16-24,25-17-9-3-10-18-25)26-19-11-4-12-20-26/h1-20,22H,21H2
InChI key
INKMLGJBBDRIQR-UHFFFAOYSA-N
应用
Reactant for:
- Tributylphosphine-mediated vinylogous Wittig reactions
- Synthesis of 1,2-dioxanes for antitrypanosomal activity
- Organocatalytic Michael-type reactions / Wittig reactions of phosphorus ylides and unsaturated ketones
- Stereoselective phosphine-catalyzed cycloaddition to form spirocyclopenteneoxindoles
- Enantioselective synthesis of pantothenic acid
- Preparation of phosphorus ylides from phosphoranes and acetic anhydride
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
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