5-(4-chlorophenyl)-2-phenyl-3-pyrazolamine

5-(4-chlorophenyl)-2-phenyl-3-pyrazolamine - Names and Identifiers

Name	5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE
Synonyms	SALOR-INT L317950-1EA 5-(4-chlorophenyl)-2-phenyl-3-pyrazolamine 5-(4-chlorophenyl)-2-phenyl-pyrazol-3-aMine 5-Amino-3-(4-chlorophenyl)-1-phenylpyrazole 3-(4-CHLOROPHENYL)-1-PHENYL-1H-PYRAZOL-5-AMINE 3-(4-chlorophenyl)-1-phenyl-1H-pyrazole-5-amine 5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE
CAS	19652-14-3
InChI	InChI=1/C15H12ClN3/c16-12-8-6-11(7-9-12)14-10-15(17)19(18-14)13-4-2-1-3-5-13/h1-10H,17H2

5-(4-chlorophenyl)-2-phenyl-3-pyrazolamine - Physico-chemical Properties

Molecular Formula	C15H12ClN3
Molar Mass	269.73
Density	1.28±0.1 g/cm3(Predicted)
Melting Point	190.0 to 194.0 °C
Boling Point	477.0±35.0 °C(Predicted)
Flash Point	242.3°C
Vapor Presure	2.91E-09mmHg at 25°C
Appearance	powder to crystal
Color	White to Yellow to Orange
pKa	2.24±0.10(Predicted)
Storage Condition	Room Temprature
Refractive Index	1.659

5-(4-chlorophenyl)-2-phenyl-3-pyrazolamine - Introduction

5-(4-chlo-orphenyl)-is an organic compound with the molecular formula C17H12ClN3. The following is an introduction to its nature, use, formulation and safety information:

Nature:
-Appearance: Colorless or light yellow crystal
-Melting point: about 170-172 ° C
-Solubility: Slightly soluble in water, soluble in other organic solvents such as ethanol, dimethyl ether, etc.
-Chemical properties: The compound has certain pharmaceutical activity and can be used as a precursor or intermediate of anti-tumor, antibacterial and antifungal drugs.

Use:
-Pharmaceutical use: The compound is widely used in the pharmaceutical field and can be used as a synthetic intermediate for anti-tumor, antibacterial and antifungal drugs. It has important application value in the research and development of new drugs.
-Research use: The compound is also used in organic chemistry research as a reference substance or reagent.

Method:
-The synthesis of this compound is usually carried out through a multi-step reaction. For example, starting from benzoic acid, it can be converted into the target compound through catalytic hydrogenation, diazotization, coupling reaction and other steps.

Safety Information:
-Follow laboratory safety regulations and wear appropriate protective equipment such as lab gloves, glasses, etc. when handling and handling the compound.
-Because the compound has certain toxicity and irritation, avoid inhaling aerosols or dust, and avoid contact with skin and eyes.
-When using or disposing of the compound, comply with local laws and regulations and properly dispose of waste to prevent adverse effects on humans and the environment.

Please note that the above content is for reference only, and relevant regulations and safety operation guidelines should be followed when using this compound.

Last Update：2024-04-09 21:04:16