122806-25-1

Basic information

• Product Name: Ethanone, 1-(3-methoxyphenyl)-, oxime
• CAS NO: 122806-25-1
• Molecular Formula: C9H11NO2
• Molecular Weight: 165.192
• Mol File: 122806-25-1.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(3-methoxyphenyl)-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-methoxyphenyl)-, oxime(122806-25-1)
• EPA Substance Registry System: Ethanone, 1-(3-methoxyphenyl)-, oxime(122806-25-1)

Safety Data

• Hazardous Substances Data: 122806-25-1(Hazardous Substances Data)

Upstream product

• 586-37-8 1-(3-Methoxyphenyl)ethanone 

Downstream Products

• 50919-07-8 1-(3-methoxy-phenyl)-ethylamine 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 588-16-9 m-methoxyacetanilide 
• 905458-53-9 P,P-diphenyl-N-[1-(3-methoxyphenyl)ethylidene]phosphinic amide 
• 1198575-40-4 1-methyl-7-methoxy-3,4-diphenylisoquinoline 
• 1234693-05-0 (R)-2-methoxy-N-[1-(3-methoxyphenyl)ethyl]acetamide 
• 35129-32-9 N-methyl-3-methoxybenzamide 
• 1244768-87-3 (E)-N-(1-(1H-benzo[d][1,2,3]triazol-1-yl)ethylidene)-3-methoxyaniline 
• 1333120-04-9 2,6-bis(3-methoxylphenyl)-4-phenylpyridine 
• 896868-57-8 1-(3-methoxyphenyl)ethanone O-acetyl oxime 
• 329697-55-4 1,2-bis[1-(3-methoxyphenyl)ethylidene]hydrazine 
• 1604842-44-5 C₁₇H₁₉NO₅ 
• 1285694-86-1 2,4-bis(3-methoxyphenyl)pyridine 
• 76143-84-5 7-methoxy-1-methylisoquinoline 

Relevant articles and documents

Chemoenzymatic synthesis of the calcimimetics (+)-NPS R-568 via asymmetric reductive acylation of ketoxime intermediate

A practical and efficient procedure for the synthesis of a potent calcimimetic (+)-NPS R-568 was developed. This procedure includes as the key step the asymmetric reductive acylation of a ketoxime intermediate catalyzed by a Pd nanocatalyst and a lipase i

Rhodium(III)-Catalyzed Direct C-H Arylation of Various Acyclic Enamides with Arylsilanes

The stereoselective β-C(sp2)-H arylation of various acyclic enamides with arylsilanes via Rh(III)-catalyzed cross-coupling reaction was illustrated. The methodology was characterized by extraordinary efficacy and stereoselectivity, a wide scope of substrates, good functional group tolerance, and the adoption of environmentally friendly arylsilanes. The utility of this present method was evidenced by the gram-scale synthesis and further elaboration of the product. In addition, Rh(III)-catalyzed C-H activation is considered to be the critical step in the reaction mechanism.

Rhodium(iii)-catalyzed asymmetric [4+1] spiroannulations of: O -pivaloyl oximes with α-diazo compounds

Chiral RhIII catalysts can catalyze the asymmetric [4+1] spiroannulation of O-pivaloyl oximes with α-diazo homophthalimides under redox-neutral and acid/base-neutral conditions, leading to formation of chiral spirocyclic imines as a result of C-H activation and N-O cleavage. The reaction proceeded with high efficiency and features broad substrate scope, mild reaction conditions, and high to excellent enantioselectivities. This journal is