Undecylenoyl chloride
Undecylenoyl chloride structure
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Common Name | Undecylenoyl chloride | ||
|---|---|---|---|---|
| CAS Number | 38460-95-6 | Molecular Weight | 202.721 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 252.2±0.0 °C at 760 mmHg | |
| Molecular Formula | C11H19ClO | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 93.3±0.0 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Photochemically modified diamond-like carbon surfaces for neural interfaces.
Mater. Sci. Eng. C. Mater. Biol. Appl. 58 , 1199-206, (2015) Diamond-like carbon (DLC) was modified using a UV functionalization method to introduce surface-bound amine and aldehyde groups. The functionalization process rendered the DLC more hydrophilic and significantly increased the viability of neurons seeded to the... |
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Olefin cross-metathesis as a source of polysaccharide derivatives: cellulose ω-carboxyalkanoates.
Biomacromolecules 15(1) , 177-87, (2014) Cross-metathesis has been shown for the first time to be a useful method for the synthesis of polysaccharide derivatives, focusing herein on preparation of cellulose ω-carboxyalkanoates. Commercially available cellulose esters were first acylated with 10-unde... |
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Preparation of cyclodextrin-modified monolithic hybrid columns for the fast enantioseparation of hydroxy acids in capillary liquid chromatography.
J. Sep. Sci. 39 , 1110-7, (2016) Cyclodextrins and their derivatives are one of the most common and successful chiral selectors. However, there have been few publications about the use of cyclodextrin-modified monoliths. In this study, organic hybrid monoliths were prepared by the immobiliza... |
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Core crosslinkable polymeric micelles from PEG-lipid amphiphiles as drug carriers. Tian L, et al.
J. Mater. Chem. 14(14) , 2317-24, (2004)
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Enhancement of the impact strength of cationically cured cycloaliphatic diepoxide by adding hyperbranched poly (glycidol) partially modified with 10-undecenoyl chains. Flores M, et al.
Eur. Polymer J. 49(6) , 1610-20, (2013)
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