93845-93-3

Basic information

• Product Name: Cyclohexanol, 2-(4-methyl-2-quinolinyl)-
• CAS NO: 93845-93-3
• Molecular Formula: C16H19NO
• Molecular Weight: 241.333
• Mol File: 93845-93-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 2-(4-methyl-2-quinolinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 2-(4-methyl-2-quinolinyl)-(93845-93-3)
• EPA Substance Registry System: Cyclohexanol, 2-(4-methyl-2-quinolinyl)-(93845-93-3)

Safety Data

• Hazardous Substances Data: 93845-93-3(Hazardous Substances Data)

Upstream product

• 491-35-0 C₆H₄NCH₂CHCCH₂ 
• 67-64-1 acetone 
• 110-83-8 cyclohexene 
• 28141-32-4 2-Iodo-cyclohexanol 
• 143671-61-8 4-methylquinoline trifluoroacetate 
• 20668-24-0 4-Methylchinolin-2-d⁽¹⁾ 

Downstream Products

• 106719-56-6 2-(cyclohexen-1′-yl)-4-methylquinoline 

Relevant articles and documents

Visible-light-mediated three-component Minisci reaction for heteroarylethyl alcohols synthesis

Methods for heteroarylethyl alcohol synthesis are critical to the chemical and pharmaceutical industries. Herein, we report a mild, modular, practical Minisci reaction for catalytic synthesis of heteroarylethyl alcohols via sequential addition of H2O and N-heteroarenes across olefinic double bonds. This scalable protocol was used for direct hydroxy-heteroarylation of olefins with a wide range of N-heteroarenes and can be expected to permit rapid conversion of abundant feedstock materials into medically relevant molecules.

A NEW GENERAL METHOD OF HOMOLYTIC ALKYLATION OF PROTONATED HETEROAROMATIC BASES

Alkyl iodides and benzoyl peroxides provide a new general method of homolytic alkylation of protonated heteroaromatic bases.Yields are good and the substitution is selective in the positions ortho and para to the heteroatom.

POLAR EFFECTS IN FREE-RADICAL REACTIONS. A NEW TYPE OF HOMOLYTIC AROMATIC ALKYLATION BY SILVER CATALYZED OXIDATION OF ACETONE BY PEROXYDISULPHATE IN THE PRESENCE OF OLEFINS.

Silver catalyzed peroxydisulphate oxidation of acetone in the presence of olefins and protonated heteroaromatic bases leads to compound I via addition of acetonyl radical to the olefin and scavenging of the resulting radical adduct by the aromatic base.