3362-43-4

Basic information

• Product Name: Methanone, diphenyl-, O-(phenylmethyl)oxime
• CAS NO: 3362-43-4
• Molecular Formula: C20H17NO
• Molecular Weight: 287.361
• Mol File: 3362-43-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Methanone, diphenyl-, O-(phenylmethyl)oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, diphenyl-, O-(phenylmethyl)oxime(3362-43-4)
• EPA Substance Registry System: Methanone, diphenyl-, O-(phenylmethyl)oxime(3362-43-4)

Safety Data

• Hazardous Substances Data: 3362-43-4(Hazardous Substances Data)

Upstream product

• 119-61-9 benzophenone 
• 622-33-3 N-benzyloxyamine 
• 620-05-3 iodomethylbenzene 
• 98-80-6 phenylboronic acid 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 960-16-7 tributylphenylstannane 
• 100-44-7 benzyl chloride 
• 29127-86-4 benzophenone oxime ; sodium salt 
• 100-39-0 benzyl bromide 
• 574-66-3 Benzophenone oxime 
• 1013-88-3 Benzophenone imine 

Downstream Products

• 30081-56-2 1,3,4-triphenylisoquinoline 
• 387862-67-1 1-phenyl-3,4-dipropylisoquinoline 
• 1352638-38-0 3-isopropyl-4-methyl-1-phenylisoquinoline 
• 1352638-50-6 4-isopropyl-3-methyl-1-phenylisoquinoline 
• 1352638-37-9 4-methyl-3-pentyl-1-phenylisoquinoline 
• 1352638-49-3 3-methyl-4-pentyl-1-phenylisoquinoline 
• 1352638-39-1 3-isopropyl-4-(methoxymethyl)-1-phenylisoquinoline 
• 1352638-51-7 4-isopropyl-3-(methoxymethyl)-1-phenylisoquinoline 
• 1295521-98-0 1,3-diphenyl-4-propylisoquinoline 
• 75097-27-7 3-n-propyl-1,4-diphenylisoquinoline 
• 1013-88-3 Benzophenone imine 
• 574-66-3 Benzophenone oxime 
• 108-88-3 toluene 
• 100-51-6 benzyl alcohol 

Relevant articles and documents

Palladium-catalyzed cross coupling reaction of N-alkoxyimidoyl bromides and its application to one-pot synthesis of N-arylamines

The synthetic utility of N-alkoxyimidoyl halides is demonstrated using the palladium-catalyzed cross-coupling reaction. The Sonogashira and Suzuki-Miyaura coupling reactions of N-alkoxyimidoyl bromides produced versatile ketoxime ethers in good to excelle

N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction

N-Alkoxyimidoyl bromides have been successfully employed as an efficient organic partner in the Pd-catalyzed Stille coupling reaction with various organotin compounds, and the corresponding O-alkyloximes were obtained in good to excellent yields.

Synthesis of oxime esters and ethers as potential psychotropic agents.

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