1434602-02-4

Basic information

• Product Name: (E)-1-(2-fluorophenyl)ethan-1-one oxime
• Synonyms: (E)-1-(2-fluorophenyl)ethan-1-one oxime
• CAS NO: 1434602-02-4
• Molecular Weight: 153.156
• Mol File: 1434602-02-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-fluorophenyl)ethan-1-one oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-fluorophenyl)ethan-1-one oxime(1434602-02-4)
• EPA Substance Registry System: (E)-1-(2-fluorophenyl)ethan-1-one oxime(1434602-02-4)

Safety Data

• Hazardous Substances Data: 1434602-02-4(Hazardous Substances Data)

Upstream product

• 445-27-2 2'-Fluoroacetophenone 

Downstream Products

• 1434602-30-8 1-(2-fluorophenyl)ethanone O-benzyloxime 
• 185545-90-8 (R)-2-fluoro-α-methylbenzylamine 
• 68285-25-6 (S)-1-(2-fluorophenyl)ethylamine 

Relevant articles and documents

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USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS II

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N,O-Bidentate directing-enabled, traceless heterocycle synthesis is described via Cp?-free cobalt-catalyzed C-H activation/annulation. The weakly coordinating nature of the carboxylic acid was employed for the preparation of isoquinolines. Meanwhile, the N-O bond of the α-imino-oxy acid can serve as an internal oxidant. Terminal as well as internal alkynes can be efficiently applied to the catalytic system. This operationally simple approach shows a broad substrate scope with the products obtained in good to excellent yields.