Ethyl benzoate
Ethyl benzoate structure
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Common Name | Ethyl benzoate | ||
|---|---|---|---|---|
| CAS Number | 93-89-0 | Molecular Weight | 150.174 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 211.7±8.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O2 | Melting Point | -34 °C | |
| MSDS | Chinese USA | Flash Point | 84.4±0.0 °C | |
| Symbol |
GHS09 |
Signal Word | ||
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Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins
Bioorg. Med. Chem. 17 , 896-904, (2009) This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the mole... |
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Late progamic phase and fertilization affect calreticulin expression in the Hyacinthus orientalis female gametophyte.
Plant Cell Rep. 34 , 2201-15, (2015) Calreticulin expression is upregulated during sexual reproduction of Hyacinthus orientalis, and the protein is localized both in the cytoplasm and a highly specialized cell wall within the female gametophyte. Several evidences indicate calreticulin (CRT) as a... |
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Microtensile Bond Strength and Micromorphology of Bur-cut Enamel Using Five Adhesive Systems.
J. Adhes. Dent. 17 , 107-16, (2015) This study compared the microtensile bond strengths (μTBS) of two etch-and-rinse (ER) (OptiBond FL [OBFL]; Prime & Bond NT [PBNT]) and three self-etching (SE) (Clearfil SE Bond [CSEB]; Xeno III [XIII]; Xeno V+ [XV+]) adhesives systems to bur-prepared human en... |
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Effect of ionic liquids on the interaction between liposomes and common wastewater pollutants investigated by capillary electrophoresis.
J. Chromatogr. A. 1405 , 178-87, (2015) The effect of three phosphonium and imidazolium ionic liquids (ILs) on the interaction between liposomes and common pharmaceuticals found in wastewaters was studied. The liposomes comprised zwitterionic phosphatidyl choline and negatively charged phosphatidyl... |
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Thienylhalomethylketones: Irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools
Bioorg. Med. Chem. 17 , 6914-25, (2009) Thienylhalomethylketones, whose chemical, biological, and pharmaceutical data are here reported, are the first irreversible inhibitors of GSK-3beta described to date. Their inhibitory activity is likely related to the cysteine residue present in the ATP-bindi... |
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Organoleptic Characteristics of Flavor Materials Mosciano, G.
Perfum. Flavor. 4th ed., 28 , 102, (2003)
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