Patent classifications
C07D265/16
Bioderived benzoxazines
The present disclosure relates to a composition having a structure that includes ##STR00001##
where R.sub.1 includes at least one of hydrogen, carbon, and/or fluorine, and includes a covalent bond. In some embodiments of the present disclosure, R.sub.1 may include at least one of hydrogen, fluorine, a carboxyl group, a hydroxyl group, an alkoxy group, and/or a hydrocarbon chain. In some embodiments of the present disclosure, the composition may be derived from at least one of ##STR00002##
In some embodiments of the present disclosure, at least a portion of the composition may be bioderived.
Alpha-5 beta-1 inhibitors
The disclosure provides, inter alia, alpha-5 beta-1 inhibitors, pharmaceutical compositions comprising alpha-5 beta-1 inhibitors, methods for treating diseases using alpha-5 beta-1 inhibitors, and processes for making alpha-5 beta-1 inhibitors.
Benzoxazine Derivatives Vitrimers
Disulfide-containing benzoxazine monomers of formula I
##STR00001##
Also a process for synthesizing a disulfide-containing benzoxazine monomer of formula I comprises the following steps consisting of providing a mixture comprising an amino disulfide compound:H.sub.2N—R—NH.sub.2, wherein R is as defined for the monomer of formula I, an aldehyde derivative; phenolic derivatives, stirring the mixture under a temperature of from 50° C. to 130° C. for 1 h to 48 h, for obtaining the monomer of formula I; wherein the respective stoichiometry of the amino disulfide compound: aldehyde derivative:phenolic derivatives is 1:4: x.sub.1+x.sub.2, with x.sub.1+x.sub.2=2 and 0<x.sub.1;x.sub.2<2. Also a process for preparing a polybenzoxazine derivative vitrimer comprising a polymerization of the benzoxazine monomer at temperatures within the range of from 100° C. to 250° C. for 1 h to 24 h, for obtaining the polybenzoxazine derivatives vitrimer. Also polybenzoxazine derivative vitrimers, presenting at least one of the following characteristics of Tg values of from 0° C. to 250° C.; and relaxation temperature values, above the Tg values, of from 0° C. to 250° C.
Benzoxazine Derivatives Vitrimers
Disulfide-containing benzoxazine monomers of formula I
##STR00001##
Also a process for synthesizing a disulfide-containing benzoxazine monomer of formula I comprises the following steps consisting of providing a mixture comprising an amino disulfide compound:H.sub.2N—R—NH.sub.2, wherein R is as defined for the monomer of formula I, an aldehyde derivative; phenolic derivatives, stirring the mixture under a temperature of from 50° C. to 130° C. for 1 h to 48 h, for obtaining the monomer of formula I; wherein the respective stoichiometry of the amino disulfide compound: aldehyde derivative:phenolic derivatives is 1:4: x.sub.1+x.sub.2, with x.sub.1+x.sub.2=2 and 0<x.sub.1;x.sub.2<2. Also a process for preparing a polybenzoxazine derivative vitrimer comprising a polymerization of the benzoxazine monomer at temperatures within the range of from 100° C. to 250° C. for 1 h to 24 h, for obtaining the polybenzoxazine derivatives vitrimer. Also polybenzoxazine derivative vitrimers, presenting at least one of the following characteristics of Tg values of from 0° C. to 250° C.; and relaxation temperature values, above the Tg values, of from 0° C. to 250° C.
BENZOXAZINES AND COMPOSITIONS CONTAINING THE SAME
A curable composition containing more than 80% by weight of a blend of benzoxazines, wherein the blend includes (A) one or more multifunctional benzoxazines and (B) a liquid, non-halogenated monofunctional benzoxazine. This composition has been found to be stable at high temperatures, e.g. 180° C.-250° C., and suitable for making composite materials using conventional techniques such as prepregging and liquid resin infusion.
BENZOXAZINES AND COMPOSITIONS CONTAINING THE SAME
A curable composition containing more than 80% by weight of a blend of benzoxazines, wherein the blend includes (A) one or more multifunctional benzoxazines and (B) a liquid, non-halogenated monofunctional benzoxazine. This composition has been found to be stable at high temperatures, e.g. 180° C.-250° C., and suitable for making composite materials using conventional techniques such as prepregging and liquid resin infusion.
POLYMERIZABLE COMPOUND AND OPTICALLY ANISOTROPIC OBJECT
The present invention aims to provide a polymerizable compound that has high storage stability without causing crystal precipitation when added to a polymerizable composition and to provide a polymerizable composition containing the polymerizable compound. A polymer film produced by polymerization of the polymerizable composition has a low haze, high thickness uniformity, low occurrence of nonuniform orientation, high surface hardness, high adhesiveness, and good appearances and fewer orientation defects even after ultraviolet irradiation. The present invention also aims to provide a polymer produced by polymerization of the polymerizable composition and an optically anisotropic body produced from the polymer.
Use of tetrahydrobenzoxazines as stabilisers
The use of tetrahydrobenzoxazines I ##STR00001##
where R.sup.1 is a hydrocarbyl radical and R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are each independently hydrogen atoms, hydroxyl groups or hydrocarbyl radicals, and where R.sup.2 to R.sup.5 may also form a second and a third tetrahydrooxazine ring, with the proviso that at least one of the substituents has from 4 to 3000 carbon atoms and the remaining substituents, when they are hydrocarbyl radicals, each have from 1 to 20 carbon atoms, as stabilizers for stabilizing inanimate organic material, especially turbine fuels, against the action of light, oxygen and heat.
Use of tetrahydrobenzoxazines as stabilisers
The use of tetrahydrobenzoxazines I ##STR00001##
where R.sup.1 is a hydrocarbyl radical and R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are each independently hydrogen atoms, hydroxyl groups or hydrocarbyl radicals, and where R.sup.2 to R.sup.5 may also form a second and a third tetrahydrooxazine ring, with the proviso that at least one of the substituents has from 4 to 3000 carbon atoms and the remaining substituents, when they are hydrocarbyl radicals, each have from 1 to 20 carbon atoms, as stabilizers for stabilizing inanimate organic material, especially turbine fuels, against the action of light, oxygen and heat.
Polymerizable compound and optically anisotropic object
The present invention aims to provide a polymerizable compound that has high storage stability without causing crystal precipitation when added to a polymerizable composition and to provide a polymerizable composition containing the polymerizable compound. A polymer film produced by polymerization of the polymerizable composition has a low haze, high thickness uniformity, low occurrence of nonuniform orientation, high surface hardness, high adhesiveness, and good appearances and fewer orientation defects even after ultraviolet irradiation. The present invention also aims to provide a polymer produced by polymerization of the polymerizable composition and an optically anisotropic body produced from the polymer.