质量水平
检测方案
96%
形式
liquid
折射率
n20/D 1.413 (lit.)
bp
80 °C/25 mmHg (lit.)
密度
1.34 g/mL at 25 °C (lit.)
SMILES字符串
COP(Cl)(=O)OC
InChI
1S/C2H6ClO3P/c1-5-7(3,4)6-2/h1-2H3
InChI key
NGFFLHMFSINFGB-UHFFFAOYSA-N
应用
氯磷酸二甲酯可用于通过与氰基丙酮酸乙酯的烯醇钾盐反应制备 ( E )-3-氰基磷酸烯醇丙酮酸。可用于合成 2-花生四烯酸甘油醚的单磷酸酯和二磷酸酯。
警示用语:
Danger
危险分类
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
闪点(°F)
235.4 °F
闪点(°C)
113 °C
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Journal of medicinal chemistry, 46(23), 5083-5086 (2003-10-31)
The poor aqueous solubility of 2-arachidonyl glyceryl ether (noladin ether) 2 hinders both pharmacological studies and pharmaceutical development. The synthesized mono- and diphosphate esters of noladin ether (4 and 6) considerably increased the aqueous solubility of noladin ether (>40000-fold), showed
Langmuir : the ACS journal of surfaces and colloids, 28(30), 10962-10967 (2012-07-12)
The fundamental interactions of dimethyl methylphosphonate (DMMP) and dimethyl chlorophosphate (DMCP) on amorphous silica nanoparticles have been investigated with transmission infrared spectroscopy and temperature-programmed desorption (TPD). DMMP and DMCP both adsorb molecularly to silica through the formation of hydrogen bonds
Biochemistry, 24(26), 7602-7606 (1985-12-17)
(E)-3-Cyanophosphoenolpyruvate has been synthesized by reacting dimethyl chlorophosphate with the potassium enolate of ethyl cyanopyruvate. The resulting trialkyl ester was deesterified with bromotrimethylsilane followed by potassium hydroxide. Subsequent treatment with Dowex-50-H+ resin and cyclohexylamine afforded the tricyclohexylammonium salt; only the
ACS applied materials & interfaces, 11(8), 7686-7694 (2019-02-16)
Quorum sensing (QS) inhibitor-based therapy is an attractive strategy to inhibit bacterial biofilm formation without excessive induction of antibiotic resistance. Thus, we designed Ca2+-binding poly(lactide- co-glycolide) (PLGA) microparticles that can maintain a sufficient concentration of QS inhibitors around hydroxyapatite (HA)
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