The invention claimed is:
1. A monoglycidyl isocyanurate compound of Formula (3) below:
wherein two R 2 s are each a C 1-5 alkylene group, two R 4 s are each a C 1-2 alkylene group, and two R 5 s are each a C 1-2 alkyl group.
2. The monoglycidyl isocyanurate compound according to claim 1 , wherein the two R 2 s are each a C 1-2 alkylene group.
3. The monoglycidyl isocyanurate compound according to claim 1 , wherein the monoglycidyl isocyanurate compound of Formula (3) is liquid at normal temperature under normal pressure when the total number of carbon atoms and oxygen atoms of a —R 2 OR 4 OR 5 group in Formula (3) is four or more.
4. A method for producing the monoglycidyl isocyanurate compound according to claim 1 comprising the steps of obtaining a reaction intermediate of the following Formula (3′):
wherein two R 2 s, two R 4 s, and two R 5 s each have the same definition as that in claim 1 from monoallyl isocyanuric acid, and reacting the reaction intermediate of Formula (3′) with an oxidant.
5. The method for producing the monoglycidyl isocyanurate compound according to claim 4 , wherein the reaction intermediate of Formula (3′) is obtained by reacting the monoallyl isocyanuric acid with a compound of the following Formula (c):
wherein X is a chloro group, a bromo group, or an iodo group, and R 2 is a C 1-5 alkylene group, R 4 is a C 1-2 alkylene group, and R 5 is a C 1-2 alkyl group.
6. The method for producing the monoglycidyl isocyanurate compound according to claim 4 , wherein the oxidant is m-chloroperbenzoic acid or hydrogen peroxide.