C07D303/18

High heat monomers and methods of use thereof

High purity epoxide compounds methods for preparing the high purity epoxide compounds, and compositions derived from the epoxide compounds are provided. Also provided are materials and articles derived from the epoxide compounds.

Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium

A fluorine-containing ether compound of the present invention is represented by Formula (1).
R.sup.1CH.sub.2R.sup.2CH.sub.2R.sup.3(1) (In Formula (1), R.sup.1 is an organic end group having 3 or more carbon atoms which includes two or more polar groups with each polar group being bonded to different carbon atoms and the carbon atoms to which the polar groups are bonded being bonded to each other via a linking group including the carbon atoms which are not bonded to the polar groups, R.sup.2 includes a perfluoropolyether chain represented by Formula (3), and R.sup.3 is a hydroxyl group or R.sup.1)
(CF.sub.2).sub.y1O((CF.sub.2).sub.yO).sub.z(CF.sub.2).sub.y1(3) (In Formula (3), y represents an integer of 2 to 4, and z represents an integer of 1 to 30).

Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium

A fluorine-containing ether compound of the present invention is represented by Formula (1).
R.sup.1CH.sub.2R.sup.2CH.sub.2R.sup.3(1) (In Formula (1), R.sup.1 is an organic end group having 3 or more carbon atoms which includes two or more polar groups with each polar group being bonded to different carbon atoms and the carbon atoms to which the polar groups are bonded being bonded to each other via a linking group including the carbon atoms which are not bonded to the polar groups, R.sup.2 includes a perfluoropolyether chain represented by Formula (3), and R.sup.3 is a hydroxyl group or R.sup.1)
(CF.sub.2).sub.y1O((CF.sub.2).sub.yO).sub.z(CF.sub.2).sub.y1(3) (In Formula (3), y represents an integer of 2 to 4, and z represents an integer of 1 to 30).

Polymer-conjugated METAP2 inhibitors, and therapeutic methods of use thereof
10722532 · 2020-07-28 · ·

One aspect of the invention provides polymer conjugated MetAP2 inhibitors. While not being bound by any particular theory, it is believed that coupling the MetAP2 inhibitory core via the linkers described herein provides compounds with superior efficacy to the parent small molecules and superior pharmacokinetic profiles. In one aspect of the invention, the polymer conjugated MetAP2 inhibitors are useful in methods of treating disease, comprising administering to a subject in need thereof a therapeutically effective amount of a polymer conjugated MetAP2 inhibitor.

Polymer-conjugated METAP2 inhibitors, and therapeutic methods of use thereof
10722532 · 2020-07-28 · ·

One aspect of the invention provides polymer conjugated MetAP2 inhibitors. While not being bound by any particular theory, it is believed that coupling the MetAP2 inhibitory core via the linkers described herein provides compounds with superior efficacy to the parent small molecules and superior pharmacokinetic profiles. In one aspect of the invention, the polymer conjugated MetAP2 inhibitors are useful in methods of treating disease, comprising administering to a subject in need thereof a therapeutically effective amount of a polymer conjugated MetAP2 inhibitor.

LINKER COMPOUNDS, METHODS OF PRODUCING THE SAME AND USES THEREOF
20200087238 · 2020-03-19 ·

The present disclosure provides a bifunctional linker for coupling at least one functional moiety, preferably a bis-allyl propionic acid (BAPA), to a polymer-containing matrix. Also disclosed by the present disclosure are anhydrides of the bifunctional linker, processes for preparing the bifunctional linker and such anhydride, as well as surfaces, such as cellulose containing matrices, coupled with the bifunctional linker, at times, the latter carrying a functional agent.

LINKER COMPOUNDS, METHODS OF PRODUCING THE SAME AND USES THEREOF
20200087238 · 2020-03-19 ·

The present disclosure provides a bifunctional linker for coupling at least one functional moiety, preferably a bis-allyl propionic acid (BAPA), to a polymer-containing matrix. Also disclosed by the present disclosure are anhydrides of the bifunctional linker, processes for preparing the bifunctional linker and such anhydride, as well as surfaces, such as cellulose containing matrices, coupled with the bifunctional linker, at times, the latter carrying a functional agent.

PHENALENE-1-ONE-CONTAINING PHOTOSENSITIZER COMPOSITION, PHENALENE-1-ONE COMPOUND AND THE USE THEREOF
20200087259 · 2020-03-19 ·

A phenalene-1-one compound, a photosensitizer composition including the phenalene-1-one compound, an article including the phenalene-1-one compound and/or photosensitizer composition and the use thereof.

PHENALENE-1-ONE-CONTAINING PHOTOSENSITIZER COMPOSITION, PHENALENE-1-ONE COMPOUND AND THE USE THEREOF
20200087259 · 2020-03-19 ·

A phenalene-1-one compound, a photosensitizer composition including the phenalene-1-one compound, an article including the phenalene-1-one compound and/or photosensitizer composition and the use thereof.

HIGH HEAT MONOMERS AND METHODS OF USE THEREOF
20200010608 · 2020-01-09 ·

High purity epoxide compounds methods for preparing the high purity epoxide compounds, and compositions derived from the epoxide compounds are provided. Also provided are materials and articles derived from the epoxide compounds.