69731-45-9

Usage

Uses

Due to the limited information available, it is difficult to list specific applications for 1,3-bis(oxiranylmethyl)-5-(2-propenyl)-1,3,5-Triazine-2,4,6(1H,3H,5H)-trione. However, given the functional groups present in its structure, it is possible that it could be used in various chemical reactions or as a component in the synthesis of other compounds. Further research and investigation would be required to determine its potential uses in different industries.

Upstream product

• 1025-15-6 triallyl isocyanurate 
• 3030-60-2 propenyl-1,3,5-triazine-2,4,6-(1H,3H,5H)trione 
• 106-89-8 epichlorohydrin 

Relevant academic research and scientific papers

Dual-reactive hyperbranched polymer synthesis through proton transfer polymerization of thiol and epoxide groups

A new synthesis of hyperbranched polymers through proton transfer polymerization of thiol and epoxide groups is presented. For this, an AB 2 monomer bearing two epoxides and a thiol groups is synthesized. Base-catalyzed proton transfer polymerization of this monomer led to the formation of a polythioether-based hyperbranched polymer with a 65-69% degree of branching and carrying about 2% of disulfide-based structural defects. This polymer contained two reactive sites, a hydroxyl group and an epoxide unit, distributed throughout the branched scaffold. The epoxide groups could be employed in anchoring an alkyl, aryl, or ethylene oxide chain through a thiol-epoxy reaction, while the hydroxyl groups produced during the polymerization and the first functionalization reactions could be engaged in attaching positively charged primary ammonium groups to the branched backbone. These sequential postpolymerization modifications transformed the general dual-reactive scaffold into dual-functionalized hyperbranched materials with potential utility in the arena of gene delivery applications.

Epoxy compound using thiol-ene reaction and method for preparing the same, and composite of organic-inorganic materials comprising a cured product thereof and method for preparing the composite

The present invention relates to: an epoxy compound having an alkoxysilyl alkyl-S-alkyl group; a manufacturing method thereof; an organic-inorganic material composite including a cured product thereof; and a method for manufacturing the composite, and mor

Epoxy compound using thiol-ene reaction and method for preparing the same, and composite of organic-inorganic materials comprising a cured product thereof and method for preparing the composite

The present invention relates to an epoxy compound having an alkoxysilylalkyl-S-alkyl group and a method for preparing the same, and a composite of organic-inorganic materials comprising a cured product thereof and a method for preparing the composite. Th

Photosensitive resin composition for color filter and uses thereof

The present invention relates to a photosensitive resin composition for a color filter and uses thereof. The photosensitive resin composition includes an alkali-soluble resin (A), a compound (B) containing an ethylenically unsaturated group, a photoinitiator (C), a pigment (D) and an organic solvent (E). The photosensitive resin composition according to the present invention can improve linearity of pattern with high finesse and developing-resistance of the color filter.

EPOXY AND ALKOXY SILYL GROUP-CONTAINING SILSESQUIOXANE AND COMPOSITION THEREOF

A silicon compound is described, being obtained by a hydrosilylation reaction of the following compound (a), compound (b) and compound (c). Compound (a) is a silsesquioxane derivative having two or more SiH in one molecule. Compound (b) is a compound having, in one molecule, epoxy and/or oxetanyl and an alkenyl having a carbon number of 2 to 18. Compound (c) is a compound having, in one molecule, an alkoxysilyl and an alkenyl having a carbon number of 2 to 18.

ISOCYANURATE EPOXY COMPOUND HAVING ALKOXYSILYL GROUP, METHOD OF PREPARING SAME, COMPOSITION INCLUDING SAME, CURED PRODUCT OF THE COMPOSITION, AND USE OF THE COMPOSITION

The present invention relates to an alkoxysilyl-based isocyanurate epoxy compound, a method of preparing same, a composition including same, a cured product of the composition and a use of the composition. A complex including the compound illustrates good heat resistance, particularly, a low coefficient of thermal expansion (CTE), and a high glass transition temperature or Tg. A cured product of the composition illustrates flame retardancy and does not use a separate silane coupling agent. According to the present invention, an isocyanurate epoxy compound including an alkoxysilyl group and an epoxy group at a core; a method of preparing the epoxy compound prepared by epoxidation and alkoxysilylation of a starting material; an epoxy composition including the epoxy compound; and a cured product of the epoxy composition and a use of the epoxy composition, are provided. In the complex of the composition including the novel alkoxysilyl-based isocyanurate epoxy compound according to the present invention, chemical bonding efficiency may be improved when making a chemical bond between the alkoxysilyl group in the epoxy compound and a filler and when forming an epoxy complex through a chemical bond between alkoxysilyl groups in the epoxy compound having the alkoxysilyl group. Therefore, good heat resistance, that is, a low CTE and a high glass transition temperature or Tg may be shown. In addition, the cured product of the composition including the epoxy compound according to the present invention may show good flame retardancy.

Isocyanuric acid derivatives, method of preparation, therapeutic compositions with a cytostatic action and therapeutic method

N-substituted-diglycidyl-isocyanurates having the formula: STR1 wherein R represents a hydrocarbon-containing radical selected from the group consisting of alkyl, aryl, aralkyl, alkaryl and cycloalkyl, optionally containing: (a) heterocycles except epoxides, and unsaturation, and (b) substituents selected from the group consisting of halogen, hydroxyl, amino, N-substituted amino, mercapto, alkylmercapto, arylmercapto, alkylsulfoxy, arylsulfoxy, alkoxy, aryloxy and acyloxy, and R1 represents a member selected from the group consisting of hydrogen and alkyl having from 1 to 4 carbon atoms, as well as the method for preparing said N-substituted-diglycidyl-isocyanurates, therapeutic compositions with cytostatic action comprising said N-substituted-diglycidyl-isocyanurates, and a method of treatment of malignant neoplasias in warm-blooded animals by administering a therapeutically effective amount of said N-substituted-diglycidyl-isocyanurate.