324-32-3

Basic information

• Product Name: 2-Methyl-7-(trifluoroMethyl)quinoline
• Synonyms: 2-Methyl-7-(trifluoroMethyl)quinoline;N-(4-IODO-2-PYRIDINYL)ACETAMIDE
• CAS NO: 324-32-3
• Molecular Formula: C₁₁H₈F₃N
• Molecular Weight: 211.1831296
• Mol File: 324-32-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-Methyl-7-(trifluoroMethyl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-7-(trifluoroMethyl)quinoline(324-32-3)
• EPA Substance Registry System: 2-Methyl-7-(trifluoroMethyl)quinoline(324-32-3)

Safety Data

• Hazardous Substances Data: 324-32-3(Hazardous Substances Data)

Usage

General Description

2-Methyl-7-(trifluoroMethyl)quinoline is a chemical compound with the molecular formula C11H8F3N. It is a heterocyclic aromatic compound that consists of a quinoline ring with a methyl group and a trifluoromethyl group attached at specific positions. 2-Methyl-7-(trifluoroMethyl)quinoline is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds. It has also been studied for its potential biological activities, including its anti-inflammatory and antifungal properties. Additionally, 2-Methyl-7-(trifluoroMethyl)quinoline is used in the field of organic chemistry as a reagent for various organic transformations and reactions. Overall, this compound plays a significant role in the development of new drug candidates and in the advancement of chemical synthesis methodologies.

Upstream product

• 98-16-8 3-trifluoromethylaniline 
• 123-73-9 crotonaldehyde 
• 402-13-1 2-amino-4-trifluoromethylbenzoic acid 
• 186602-93-7 [2-amino-4-(trifluoromethyl)phenyl]methan-1-ol 
• 123-42-2 4-Hydroxy-4-methyl-2-pentanone 
• 109466-88-8 2-amino-4-(trifluoromethyl)benzaldehyde 
• 4784-77-4 (E)-1-Bromo-2-butene 
• 588-00-1 1,2-bis(3-(trifluoromethyl)phenyl)diazene 
• 123-73-9 trans-Crotonaldehyde 

Downstream Products

• 475098-86-3 2-methylquinoline-7-carboxylic acid 
• 168083-09-8 3-(7-trifluoromethyl-2-quinolinylmethoxy)aniline 
• 168083-34-9 2-(bromomethyl)-7-(trifluoromethyl)quinoline 

Relevant articles and documents

Design, synthesis, and antibacterial evaluation of PFK-158 derivatives as potent agents against drug-resistant bacteria

Infections caused by antibiotic resistant bacteria are a major health concern throughout the world. It is well known that PFK-158 can enhance the antibacterial effect of polymyxin, but its own anti-bactericidal effect is rarely discussed. In order to inve

Copper-Promoted Tandem Reaction of Azobenzenes with Allyl Bromides via N=N Bond Cleavage for the Regioselective Synthesis of Quinolines

A copper-promoted tandem reaction of a variety of azobenzenes and allyl bromides via N=N bond cleavage to regioselectively construct quinoline derivatives has been developed. The azobenzenes act as not only construction units but also an oxidant for quinoline formation.

Use of the Kohonen neural network for rapid screening of ex vivo anti-HIV activity of styrylquinolines

Using the Kohonen neural network, the electrostatic potentials on the molecular surfaces of 14 styrylquinoline derivatives were drawn as comparative two-dimensional maps and compared with their known human immunodeficiency virus (HIV)-1 replication blocki