P-0

P-0 - Names and Identifiers

Name	Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate
Synonyms	P-0 ethyl-2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate ETHYL 2-CYCLOPROPYL-4-(4-FLUOROPHENYL)QUINOLINE-3-CARBOXYLATE Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylat... N-1 ETHYL-2-CYCLOPROPYL-4-(4-FLUOROPHENYL)-QUINOLYL-3- CARBOXYLATE 3-carboxylato-2-cyclopropyl-5-ethyl-4-(4-fluorophenyl)quinolin-6-yl 2-Cyclopropyl-4-(4-fluorophenyl)-3-quinolinecarboxylic acid ethyl ester 3-Quinolinecarboxylic acid,2-cyclopropyl-4-(4-fluorophenyl)-,ethyl ester 3-Quinolinecarboxylic acid, 2-cyclopropyl-4-(4-fluorophenyl)-, ethyl ester
CAS	148516-11-4
InChI	InChI=1/C21H18FNO2/c1-2-25-21(24)19-18(13-9-11-15(22)12-10-13)16-5-3-4-6-17(16)23-20(19)14-7-8-14/h3-6,9-12,14H,2,7-8H2,1H3

P-0 - Physico-chemical Properties

Molecular Formula	C21H18FNO2
Molar Mass	335.37
Density	1.248
Melting Point	74-76°C
Boling Point	469.2±45.0 °C(Predicted)
Flash Point	237.545°C
Vapor Presure	0mmHg at 25°C
pKa	3.54±0.50(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.627

P-0 - Introduction

Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate, abbreviated as CFPQL, is an organic compound. The following is an introduction to its nature, use, formulation and safety information:

Nature:
1. Appearance: Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate is a colorless to pale yellow liquid.
2. Melting Point: About -30 ° C.
3. Boiling Point: about 370 ° C.
4. Solubility: Soluble in many organic solvents, such as ethanol, dimethyl sulfoxide and dichloromethane.

Use:
Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate has important application value in organic synthesis and is often used to synthesize pesticides and pharmaceutical intermediates. It can also be used in organic chemistry research and laboratory synthesis reactions.

Method:
The synthesis of Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate is usually obtained by a multi-step reaction. A common synthesis method is to react 4-fluorobenzoic acid with terephthalonitrile in an ammonia atmosphere to produce 2-cyclopropyl-4-(4-fluorophenyl)-Quinoline -3-carboxylic acid, and then esterified with ethanol to produce the target product.

Safety Information:
1. Ethyl 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-carboxylate is an organic compound. Please pay attention to personal protective measures during use, such as wearing gloves and protective glasses.
2. Avoid contact with skin and eyes, if contact, should immediately rinse with plenty of water.
3. During storage and use, avoid contact with oxidants to avoid dangerous chemical reactions.
4. Please pay attention to ventilation during operation and avoid inhaling its steam.
5. If swallowed or taken by mistake, please seek medical attention immediately and bring the packaging container or label.

Last Update：2024-04-09 15:17:52