1236-90-4

Basic information

• Product Name: Quinoline, 2-(4-chlorophenyl)-4-phenyl-
• CAS NO: 1236-90-4
• Molecular Formula: C21H14ClN
• Molecular Weight: 315.802
• Mol File: 1236-90-4.mol
• Article Data: 41

Chemical Properties

• CAS DataBase Reference: Quinoline, 2-(4-chlorophenyl)-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoline, 2-(4-chlorophenyl)-4-phenyl-(1236-90-4)
• EPA Substance Registry System: Quinoline, 2-(4-chlorophenyl)-4-phenyl-(1236-90-4)

Safety Data

• Hazardous Substances Data: 1236-90-4(Hazardous Substances Data)

Usage

General Description

Quinoline, 2-(4-chlorophenyl)-4-phenyl- is a chemical compound with the molecular formula C19H13ClN. It is a derivative of quinoline and contains a chlorine atom attached to a phenyl group at the 4-position. Quinoline, 2-(4-chlorophenyl)-4-phenyl- is often used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Additionally, it has been found to exhibit potential anti-cancer properties, making it a subject of interest in the development of new drugs. Its unique structure and reactivity make it a versatile molecule with diverse potential applications in the fields of chemistry and medicine.

Upstream product

• 1018968-30-3 C₂₁H₁₆ClN 
• 104-88-1 4-chlorobenzaldehyde 
• 536-74-3 phenylacetylene 
• 62-53-3 aniline 
• 434935-80-5 rac-N-(1-(4-chlorophenyl)-3-phenyl-2-propynyl)aniline 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 
• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 16616-42-5 p-chlorobenzoylphenylacetylene 
• 137-07-5 2-amino-benzenethiol 
• 133363-44-7 N-[2-(1-phenylethenyl)phenyl]formamide 
• 2948-37-0 N-(4-chlorophenyl)benzylamine 
• 98-86-2 acetophenone 
• 57957-24-1 N-(1-phenylvinyl)acetamide 
• 2362-79-0 N-(4-chlorobenzylidene)aniline 

Relevant articles and documents

Synthesis of quinolines: Via sequential addition and I2-mediated desulfurative cyclization

An efficient one-pot approach for the synthesis of quinolines from o-aminothiophenol and 1,3-ynone under mild conditions is disclosed. With the aid of ESI-MS analysis and parallel experiments, a three-step mechanism is proposed - a two-step Michael additi

Mn(III)-Mediated Regioselective 6-endo-trig Radical Cyclization of o-Vinylaryl Isocyanides to Access 2-Functionalized Quinolines

A Mn(III)-mediated radical cyclization reaction of o-vinylaryl isocyanides and arylboronic acids or diphenylphosphine oxides to access various 2-functionalized quinolines under mild conditions was developed. With the introduction of radical stabilizing substituents (e. g. aryl and methyl group) on vinyl group, this reaction provides a regiospecific 6-endo-trig radical cyclization of o-vinylaryl isocyanides, giving a number of structurally unique and biologically potential 2-functionalized quinoline derivatives.

Magnetic Fe–Cr–Ni oxide alloy nano-belts prepared from the chemical decomposition of a stainless steel screw (a top-down approach): an efficient and cheap catalyst for multicomponent reactions

Abstract: A new, cheap, and accessible method has been used for the preparation of nano-belts from the chemical decomposition (top-down approach) of a cheap stainless steel screw and found as an efficient magnetically recyclable nanocatalyst for the prepa