53411-33-9

Basic information

• Product Name: 1-(2,4,6-Trichlorophenyl)-3-(5-amino-2-chloroanilino)-5-pyrazolone
• Synonyms: 5-(5-AMINO-2-CHLOROANILINO)-2-(2,4,6-TRICHLOROPHENYL)-2.4-DIHYDROPYRAZOL-3-ONE;5-[(5-amino-2-chlorophenyl)amino]-2,4-dihydro-2-(2,4,6-trichlorophenyl)-3h-pyrazol-3-one;3-(5-AMINO-2-CHLOROANILINO)-1-(2,4,6-TRICHLOROPHENYL)-5-PYRAZOLONE;1-(2,4,6-Trichlorophenyl)-3-(5-Amino-2-Chlorophenyl)Amino-5-Pyrazolone;1-(2,4,6-trichlorophenyl)-3-(2-chloro-5-aminoanilino)-5-pyrazolon;1-(2,4,6-Trichlorophenyl)-3-(5-Amino-2-Chloroanilino)-5-Pyrazoloone;3-(5-Amino-2-chloroanilino)-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one;5-(5-amino-2-chloro-anilino)-2-(2,4,6-trichlorophenyl)-4H-pyrazol-3-one
• CAS NO: 53411-33-9
• Molecular Formula: C15H10Cl4N4O
• Molecular Weight: 404.08
• EINECS: 258-542-0
• Mol File: 53411-33-9.mol
• Article Data: 0

Chemical Properties

• Melting Point: 237-238 °C
• Boiling Point: 545.4 °C at 760 mmHg
• Flash Point: 283.6 °C
• Appearance: /
• Density: 1.68 g/cm³
• Vapor Pressure: 2E-12mmHg at 25°C
• Refractive Index: 1.74
• Storage Temp.: 2-8°C
• PKA: 3.62±0.10(Predicted)
• CAS DataBase Reference: 1-(2,4,6-Trichlorophenyl)-3-(5-amino-2-chloroanilino)-5-pyrazolone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4,6-Trichlorophenyl)-3-(5-amino-2-chloroanilino)-5-pyrazolone(53411-33-9)
• EPA Substance Registry System: 1-(2,4,6-Trichlorophenyl)-3-(5-amino-2-chloroanilino)-5-pyrazolone(53411-33-9)

Safety Data

• Hazardous Substances Data: 53411-33-9(Hazardous Substances Data)

Usage

General Description

1-(2,4,6-Trichlorophenyl)-3-(5-amino-2-chloroanilino)-5-pyrazolone is a chemical compound that belongs to the class of pyrazolone derivatives. It is a yellow crystalline solid that is commonly used as an analytical reagent and in organic synthesis. The compound possesses antipyretic, analgesic, and anti-inflammatory properties, making it a useful ingredient in pharmaceuticals. It is also used in the detection and determination of various metal ions due to its chelating and complex-forming abilities. Additionally, it has applications in the fields of dye, pigment, and polymer chemistry. The compound’s functional groups provide it with a broad range of chemical reactivity, making it a versatile and valuable compound in various industries.

InChI:InChI=1/C15H10Cl4N4O/c16-7-3-10(18)15(11(19)4-7)23-14(24)6-13(22-23)21-12-5-8(20)1-2-9(12)17/h1-6,21-22H,20H2