等級
technical
化驗
~90% (GC)
折射率
n20/D 1.444 (lit.)
n20/D 1.444
bp
109 °C/0.4 mmHg (lit.)
密度
1.07 g/mL at 25 °C (lit.)
SMILES 字串
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 密鑰
LQZCYXCHWNQBKX-UHFFFAOYSA-N
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應用
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
其他說明
Wittig-Horner reagent for the synthesis of 1-substituted 1-octen-3-ones from aldehydes, especially for introducing the ω-chain in prostaglandins and thromboxanes
取代透過
Journal of the Chemical Society. Perkin Transactions 1, 1825-1825 (1987)
The Journal of Organic Chemistry, 54, 5128-5128 (1989)
Prostaglandins and Thromboxanes (1982)
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