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等级
technical grade
方案
85%
反应适用性
reaction type: C-C Bond Formation
折射率
n20/D 1.444 (lit.)
沸点
109 °C/0.4 mmHg (lit.)
密度
1.07 g/mL at 25 °C (lit.)
官能团
ketone
phosphonate
SMILES字符串
CCCCCC(=O)CP(=O)(OC)OC
InChI
1S/C9H19O4P/c1-4-5-6-7-9(10)8-14(11,12-2)13-3/h4-8H2,1-3H3
InChI key
LQZCYXCHWNQBKX-UHFFFAOYSA-N
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应用
前列腺素合成的关键中间体。
Reactant for:
- Beirut reaction for the preparation of phosphonylated quinoxaline dioxides
- Preparation of pyrrolomorphinan derivatives as κ opioid agonists via cyclocondensation, Vilsmeier-Haack formylation, Horner-Wadsworth-Emmons reaction, and Kocienski-modified Julia olefination from naltrexone methyl ether
- Synthesis of C-glycosides amphiphiles via solvent-free Horner-Wadsworth-Emmons reaction with unprotected sugars
- Preparation of specific inhibitors of endocannabinoid biosynthesis
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
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