4-Pentenoic anhydride

4-Pentenoic anhydride Structure
4-Pentenoic anhydride structure
Common Name 4-Pentenoic anhydride
CAS Number 63521-92-6 Molecular Weight 182.21600
Density 0.997 g/mL at 25ºC(lit.) Boiling Point 78-81ºC0.4 mm Hg(lit.)
Molecular Formula C10H14O3 Melting Point N/A
MSDS Chinese USA Flash Point 230 °F
Symbol GHS07
GHS07
Signal Word Warning

Surface Eroding, Semicrystalline Polyanhydrides via Thiol-Ene "Click" Photopolymerization.

Biomacromolecules 16 , 1650-9, (2015)

Surface eroding and semicrystalline polyanhydrides, with tunable erosion times and drug delivery pharmacokinetics largely dictated by erosion, are produced easily with thiol-ene "click" polymerization. This strategy yields both linear and cross-linked network...

Photopolymerized cross-linked thiol-ene polyanhydrides: erosion, release, and toxicity studies.

Biomacromolecules 15(7) , 2573-82, (2014)

Several critical aspects of cross-linked polyanhydrides made using thiol-ene polymerization are reported, in particular the erosion, release, and solution properties, along with their cytotoxicity toward fibroblast cells. The monomers used to synthesize these...

Thiol-yne and thiol-ene "click" chemistry as a tool for a variety of platinum drug delivery carriers, from statistical copolymers to crosslinked micelles.

Biomacromolecules 12(5) , 1738-51, (2011)

Statistical and block copolymers based on poly(2-hydroxyethyl methacrylate) (PHEMA) and poly[oligo(ethylene glycol) methylether methacrylate] (POEGMEMA) were modified with 4-pentenoic anhydride or 4-oxo-4-(prop-2-ynyloxy)butanoic anhydride to generate polymer...

Synthesis of thiol-linked neoglycopolymers and thermo-responsive glycomicelles as potential drug carrier.

Chem. Commun. (Camb.) (10) , 1198-200, (2009)

Homopolymer and block copolymer bearing carbohydrate side chain functionality were obtained by grafting glucothiose onto alkene functional scaffolds via a thiol-ene click reaction and the resulting copolymer was used to form thermo-responsive micelles as a po...

Studies of the mechanism of the hypoglycemic action of 4-pentenoic acid. Corredor C, et al.

Proc. Natl. Acad. Sci. U. S. A. 58(6) , 2299, (1967)

2-(Trimethylsilyl) ethyl Glycosides. Transformation into the Corresponding 1-O-Acyl Sugars. Ellervik U and Magnusson G.

Acta Chem. Scand. 47 , 826, (1993)