154057-56-4

154057-56-4 - Names and Identifiers

Name	3-(Bromomethyl)-2-cyclopropyl-4-(4'-fluorophenyl)quinoline
Synonyms	N-7 Br -fluorophenyl)quinoline Pitavastatin Impurity 68 2-cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-MethylBr 2-Cyclopropyl-4-(4-fluorophenyl)-quinolyl-3-MethylBroMide Quinoline,3-(broMoMethyl)-2-cyclopropyl-4-(4-fluoropenyl) 3-(bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline 3-(Bromomethyl)-2-cyclopropyl-4-(4'-fluorophenyl)quinoline 2-CYCLOPROPYL-3-(BROMOMETHYL)-4-(4-FLUOROPHENYL)-QUINOLINE Quinoline, 3-(bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)- 3-(broMoMethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline 3-(broMoMethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline
CAS	154057-56-4
EINECS	686-743-7

154057-56-4 - Physico-chemical Properties

Molecular Formula	C19H15BrFN
Molar Mass	356.23
Density	1.461±0.06 g/cm3(Predicted)
Melting Point	131-134°C
Boling Point	467.6±45.0 °C(Predicted)
Solubility	Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly, Heated)
Appearance	Solid
Color	White to Off-White
pKa	4.32±0.50(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Sensitive	Irritant
MDL	MFCD09031391

154057-56-4 - Introduction

3-(Bromomethyl)-2-cyclopropyl-4-(4 '-fluorophenyl)quinoline, also known as FBQX or Bromoquinazoline, is an organic compound with some of the following properties and uses:

Nature:
-Appearance is a white crystalline solid.
-High thermal and chemical stability.
-has a certain solubility, more easily dissolved in some organic solvents.

Use:
- 3-(Bromomethyl)-2-cyclopropyl-4-(4 '-fluorophenyl)quinoline has potential use in the pharmaceutical field and may be a candidate compound for anti-tumor and anti-cancer drugs, however, its specific efficacy and mechanism still need further study.

Method:
- 3-(Bromomethyl)-2-cyclopropyl-4-(4 '-fluorophenyl)quinoline synthesis method is more complex, a commonly used preparation method is through multi-step reaction synthesis. The specific synthesis steps include cyclization reaction of ethylene glycol dimethyl ether to obtain tetrahydroquinoline, then substitution through bromomethylation and fluorination reaction, and finally acylation and deacidification reaction of the substituted product to obtain the target product.

Safety Information: The safety and toxicity data for
- 3-(Bromomethyl)-2-cyclopropyl-4-(4 '-fluorophenyl)quinoline have not been fully established, so appropriate safety measures need to be taken during use.

Overall, 3-(Bromomethyl)-2-cyclopropyl-4-(4 '-fluorophenyl)quinoline is a potential drug compound, it may have important applications in drug research and development. However, further investigation and evaluation by the laboratory are required during use.

Last Update：2024-04-09 20:49:11

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