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4233-33-4

4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione

CAS: 4233-33-4

Molecular Formula: C8H5N3O2

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4233-33-4 - Names and Identifiers

Name 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione
Synonyms PTAD
NSC 150362
AURORA KA-3851
4-phenyl-1,2,4-triazole-3,5-dione
4-Phenyl-1,2,4-triazole-3,5-dione
4-Phenyl-1,2,4-triazoline-3,5-dione
4-PHENYL-1,2,4-TRIAZOLINE-3,5-DIONE
4-PHENYL-3H-1,2,4-TRIAZOLINE-3,5-DIONE
4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione
3H-1,2,4-Triazole-3,5(4H)-dione, 4-phenyl-
4-PHENYL-3,5-DIHYDRO-4ETA-1,2,4-TRIAZOLE-3,5-DIONE
CAS 4233-33-4
EINECS 224-191-7
InChI InChI=1/C8H5N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H
InChIKey ISULLEUFOQSBGY-UHFFFAOYSA-N

4233-33-4 - Physico-chemical Properties

Molecular FormulaC8H5N3O2
Molar Mass175.14
Density1.47±0.1 g/cm3(Predicted)
Melting Point165-170°C (dec.)(lit.)
Boling Point263.8±23.0 °C(Predicted)
Flash Point113.4°C
Solubility Chloroform (Sparingly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Sli
Vapor Presure0.0101mmHg at 25°C
AppearanceSolid
ColorRed to Dark Red
BRN141548
pKa-1.71±0.20(Predicted)
Storage Condition2-8°C
SensitiveSensitive to air
Refractive Index1.701
MDLMFCD00003148
Physical and Chemical PropertiesRose Red solid
UseHighly selective reagents for the oxidation of thiols to disulfides. Ureazole is synthesized by [3 2] cycloaddition reaction under the action of allylsilane compounds.

4233-33-4 - Risk and Safety

Safety DescriptionS22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
WGK Germany3
HS Code29339900
4233-33-4
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View History
4233-33-4
7646-93-7
142-61-0
DIBUTYLCARBAMYL CHLORIDE
PHENYL CARBONATE
GINGEROL
MAP2K1IP1
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