Cyclohexyl beta-hydroxy alkyl amines and medical uses thereof
US-2024390298-A1 · Nov 28, 2024 · US
US2016333136A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016333136-A1 |
| Application number | US-201415111337-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 9, 2014 |
| Priority date | Jan 14, 2014 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
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The present invention relates to a pyridinium-based compound of chemical formula 1, an epoxy resin composition comprising the same, and an apparatus manufactured by using the same.
Opening claim text (preview).
1 . A pyridinium-based compound represented by Formula 1: (wherein, in Formula 1, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently hydrogen, a hydroxyl group, an amino group (—NH 2 ), a nitro group (—NO 2 ), a cyano group (—CN), a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 3 to C 10 cycloalkyl group, R—C(═O)—* (where R is a C 1 to C 10 alkyl group, and * is a binding site between elements), or R′—SO 2 —* (where * is a binding site between elements, and R′ is a C 1 to C 10 alkyl group or C 6 to C 20 aryl group); R 11 and R 12 are each independently hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, or a hydroxyl group; and X is *—NR a R b (where R a and R b are each independently hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 6 to C 20 aryloxy group, or a C 7 to C 20 arylalkyl group, and * is a binding site between elements) or *—OR c (where R c is hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 6 to C 20 aryloxy group, or a C 7 to C 20 arylalkyl group, and * is a binding site between elements). 2 . The pyridinium-based compound according to claim 1 , wherein the pyridinium-based compound is represented by any one of Formulas 7 to 12: 3 . A curing catalyst represented by Formula 1: (wherein, in Formula 1, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently hydrogen, a hydroxyl group, an amino group (—NH 2 ), a nitro group (—NO 2 ), a cyano group (—CN), a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 3 to C 10 cycloalkyl group, R—C(═O)—* (where R is a C 1 to C 10 alkyl group, and * is a binding site between elements), or R′—SO 2 —* (where * is a binding site between elements, and R′ is a C 1 to C 10 alkyl group or C 6 to C 20 aryl group); R 11 and R 12 are each independently hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, or a hydroxyl group; and X is *—NR a R b (where R a and R b are each independently hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 6 to C 20 aryloxy group, or a C 7 to C 20 arylalkyl group, and * is a binding site between elements) or *—OR c (where R c is hydrogen, a C 1 to C 10 alkyl group, a C 6 to C 20 aryl group, a C 1 to C 10 alkoxy group, a C 6 to C 20 aryloxy group, or a C 7 to C 20 arylalkyl group, and * is a binding site between elements). 4 . An epoxy resin composition, comprising: an epoxy resin, a curing agent, and a curing catalyst, wherein the curing catalyst includes the pyridinium-based compound according to claim 1 . 5 . The epoxy resin composition according to claim 4 , wherein the epoxy resin includes an epoxy resin having two or more epoxy groups and one or more hydroxyl groups per molecule. 6 . The epoxy resin composition according to claim 4 , wherein the curing agent includes a phenol resin. 7 . The epoxy resin composition according to claim 4 , wherein the pyridinium-based compound is present in an amount of about 0.01 wt % to about 5 wt % in the epoxy resin composition. 8 . The epoxy resin composition according to claim 4 , wherein the pyridinium-based compound is present in an amount of about 10 wt % to about 100 wt % in the curing catalyst. 9 . The epoxy resin composition according to claim 4 , further comprising an inorganic filler. 10 . The epoxy resin composition according to claim 9 , comprising: about 2 wt % to about 17 wt % of the epoxy resin; about 0.5 wt % to about 13 wt % of the curing agent; about 70 wt % to about 95 wt % of the inorganic filler fillers; and about 0.01 wt % to about 5 wt % of the curing catalyst. 11 . An epoxy resin composition for encapsulating a semiconductor device comprising the epoxy resin composition according to claim 4 . 12 . An apparatus manufactured using the epoxy resin composition according to claim 4 .
containing organic compounds or metal hydrides · CPC title
Nitriles · CPC title
Phenols · CPC title
Oxygen atoms · CPC title
Radicals substituted by halogen atoms or nitro radicals · CPC title
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