1401733-63-8

Basic information

• Product Name: (5-methoxy-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone
• Synonyms: (5-methoxy-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone
• CAS NO: 1401733-63-8
• Molecular Weight: 283.327
• Mol File: 1401733-63-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (5-methoxy-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-methoxy-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone(1401733-63-8)
• EPA Substance Registry System: (5-methoxy-2-(1-(methoxyimino)ethyl)phenyl)(phenyl)methanone(1401733-63-8)

Safety Data

• Hazardous Substances Data: 1401733-63-8(Hazardous Substances Data)

Upstream product

• 103-50-4 dibenzyl ether 
• 72278-08-1 1-(4-Methoxy-phenyl)-ethanone O-methyl-oxime 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 100-52-7 benzaldehyde 
• 108-88-3 toluene 
• 100-51-6 benzyl alcohol 
• 98-86-2 acetophenone 
• 611-73-4 Benzoylformic acid 

Relevant articles and documents

NHPI and palladium cocatalyzed aerobic oxidative acylation of arenes through a radical process

The NHPI and palladium cocatalyzed radical oxidative acylation of arenes with aldehydes and alcohols as acyl equivalents via selective C-H functionalization has been described. Molecular oxygen, the most environmentally friendly oxidant, was used as the terminal oxidant in this catalytic cycle.

Palladium-Catalyzed Oxidative Direct ortho-C-H Acylation of Arenes with Aldehydes under Aqueous Conditions

Palladium-catalyzed ortho-acylation of arenes with aldehydes in the presence of tert-butyl hydroperoxide (TBHP) as the oxidant under aqueous conditions has been demonstrated. The acylation reaction exhibits excellent regioselectivity and wide functional g

Palladium-catalyzed direct acylation of ketoximes and aldoximes from the alcohol oxidation level through C-H bond activation

A highly efficient palladium-catalyzed oxidative ortho-acylation of O-methyl ketoximes and O-methyl aldoximes with benzylic and aliphatic alcohols from the alcohol oxidation level is described. This protocol potentially provides new opportunities to use readily available alcohols as starting materials for catalytic reactions, and represents a catalytic alternative to transcend the barriers imposed by classical Friedel-Crafts acylation. A highly efficient palladium-catalyzed oxidative ortho-acylation of O-methyl ketoximes and O-methyl aldoximes with benzylic and aliphatic alcohols from the alcohol oxidation level is described. Copyright