The 1,3,5-Triazine-2,4(1H,3H)-dione, with CAS registry number 71-33-0, belongs to the following product categories: (1)Pyridines, Pyrimidines, Purines and Pteredines; (2)All Inhibitors; (3)Bases & Related Reagents; (4)Inhibitors; (5)Nucleotides. It has the systematic name of 1,3,5-triazine-2,4(1H,3H)-dione. This chemical is a kind of crystalline solid. And this chemical is used as an antimetabolite.

Physical properties of 1,3,5-Triazine-2,4(1H,3H)-dione: (1)ACD/LogP: -1.87; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.95; (4)ACD/LogD (pH 7.4): -3.04; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1.9; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 5; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 52.98 Å²; (13)Index of Refraction: 1.748; (14)Molar Refractivity: 24.68 cm³; (15)Molar Volume: 60.6 cm³; (16)Polarizability: 9.78×10^-24cm³; (17)Surface Tension: 88.3 dyne/cm; (18)Density: 1.86 g/cm³; (19)Flash Point: 300.9 °C; (20)Enthalpy of Vaporization: 89.18 kJ/mol; (21)Boiling Point: 573.9 °C at 760 mmHg; (22)Vapour Pressure: 9.02E-14 mmHg at 25°C.

Uses of 1,3,5-Triazine-2,4(1H,3H)-dione: it can be used to produce 2-(4,6-dioxo-[1,3,5]triazinan-2-yl)-malonamide. This reaction will need solvent butan-1-ol. The yield is about 35%.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C1N\C=N/C(=O)N1
(2)InChI: InChI=1/C3H3N3O2/c7-2-4-1-5-3(8)6-2/h1H,(H2,4,5,6,7,8)
(3)InChIKey: GEWRKGDRYZIFNP-UHFFFAOYAU
(4)Std. InChI: InChI=1S/C3H3N3O2/c7-2-4-1-5-3(8)6-2/h1H,(H2,4,5,6,7,8)
(5)Std. InChIKey: GEWRKGDRYZIFNP-UHFFFAOYSA-N