30836-61-4

Basic information

• Product Name: QUINOLINE-2-YL DIPHENYL METHANOL
• Synonyms: QUINOLINE-2-YL DIPHENYL METHANOL;Quinolin-2-yl diphenyl methanol;Quinoline-yl diphenyl methanol;ALPHA,ALPHA-DIPHENYL-2-QUINOLINEMETHANOL
• CAS NO: 30836-61-4
• Molecular Formula: C₂₂H₁₇NO
• Molecular Weight: 311.38
• Mol File: 30836-61-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 494.9°C at 760 mmHg
• Flash Point: 253.1°C
• Appearance: /
• Density: 1.208g/cm³
• Vapor Pressure: 1.3E-10mmHg at 25°C
• Refractive Index: 1.676
• CAS DataBase Reference: QUINOLINE-2-YL DIPHENYL METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: QUINOLINE-2-YL DIPHENYL METHANOL(30836-61-4)
• EPA Substance Registry System: QUINOLINE-2-YL DIPHENYL METHANOL(30836-61-4)

Safety Data

• Hazardous Substances Data: 30836-61-4(Hazardous Substances Data)

Usage

General Description

QUINOLINE-2-YL DIPHENYL METHANOL is a compound with the molecular formula C25H19NO. It is a derivative of quinoline, a heterocyclic aromatic organic compound. This chemical is characterized by the presence of a quinoline group attached to a diphenyl methanol moiety. Quinoline-2-yl diphenyl methanol may have applications in the field of pharmaceuticals, as a building block for drug synthesis, or in material science research for the development of new materials with specific properties. Its structure and properties make it a potentially interesting compound for further investigation and potential uses in various industries.

InChI:InChI=1/C22H17NO/c24-22(18-10-3-1-4-11-18,19-12-5-2-6-13-19)21-16-15-17-9-7-8-14-20(17)23-21/h1-16,24H

Upstream product

• 119-61-9 benzophenone 
• 93-10-7 quinoline-2-carboxylic acid 
• 1613-37-2 Quinoline N-oxide 
• 85992-49-0 diphenyl(2-quinolyl)carbinol N-oxide 
• 91-22-5 quinoline 
• 2005-43-8 2-bromoquinoline 
• 91-63-4 2-methylquinoline 
• 5470-96-2 quinoline 2-carbaldehyde 
• 3678-74-8 2-(Diphenylmethyl)quinoline 
• 4491-33-2 ethyl quinoline-2-carboxylate 
• 75164-10-2 2-lithioquinoline 

Downstream Products

• 91-22-5 quinoline 
• 119-61-9 benzophenone 

Relevant articles and documents

Green synthesis method of polyaryl substituted methanol

The invention relates to a green synthesis method of polyaryl substituted methanol, in particular to a method for efficiently synthesizing polyaryl substituted methanol in a polar aprotic solvent under the condition of an oxidizing agent by taking polyaryl substituted methane as a raw material and alkali as an additive. The method provided by the invention is green and environment-friendly, avoids using expensive metal catalysts, and has the advantages of low cost, few reaction steps, short time, high yield and the like.

Ligand Tuning in Pyridine-Alkoxide Ligated Cp?IrIII Oxidation Catalysts

Six novel derivatives of pyridine-alkoxide ligated Cp?IrIII complexes, potent precursors for homogeneous water and C-H oxidation catalysts, have been synthesized, characterized, and analyzed spectroscopically and kinetically for ligand effects. Variation of alkoxide and pyridine substituents was found to affect their solution speciation, activation behavior, and oxidation kinetics. Application of these precursors to catalytic C-H oxidation of ethyl benzenesulfonate with aqueous sodium periodate showed that the ligand substitution pattern, solution pH, and solvent all have pronounced influences on initial rates and final conversion values. Correlation with O2 evolution profiles during C-H oxidation catalysis showed these competing reactions to occur sequentially, and demonstrates how it is possible to tune the activity and selectivity of the active species through the NO ligand structure.

Aggregative activation in heterocyclic chemistry. Part 5. Lithiation of pyridine and quinoline with the complex base BuLi·Me2N(CH2)2OLi (BuLi·LiDMAE)

It is shown that the complex base BuLi·LiDMAE reacts with pyridine to give metallated species which, after trapping by electrophiles, lead to 2-substituted pyridines in good to excellent yields. The same reactions have been less successfully performed with quinoline.