1313430-15-7

Basic information

• Product Name: C₁₀H₁₂FNO₂
• Synonyms: C₁₀H₁₂FNO₂
• CAS NO: 1313430-15-7
• Molecular Weight: 197.209
• Mol File: 1313430-15-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₀H₁₂FNO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₁₂FNO₂(1313430-15-7)
• EPA Substance Registry System: C₁₀H₁₂FNO₂(1313430-15-7)

Safety Data

• Hazardous Substances Data: 1313430-15-7(Hazardous Substances Data)

Upstream product

• 72278-08-1 1-(4-Methoxy-phenyl)-ethanone O-methyl-oxime 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 74457-86-6 1-(2-fluoro-4-methoxyphenyl)-1-ethanone 
• 593-56-6 N-methoxylamine hydrochloride 

Downstream Products

• 1313430-07-7 C₁₇H₁₆FNO₄ 
• 74457-86-6 1-(2-fluoro-4-methoxyphenyl)-1-ethanone 

Relevant articles and documents

Nitrate promoted mild and versatile Pd-catalysed C(sp2)-H oxidation with carboxylic acids

A nitrate-promoted Pd-catalysed mild cross-dehydrogenative C(sp2)-H bond oxidation of oximes or azobenzenes with diverse carboxylic acids has been developed. In contrast to the previous catalytic systems, this protocol features mild conditions (close to room temperature for most cases) and a broad substrate scope (up to 64 examples), thus constituting a versatile method to directly prepare diverse O-aryl esters. Moreover, the superiority of the nitrate additive in this mild transformation was further determined by experimental and computational evidence.

Direct sequential C-O and C-C formation via double sp2 C-H bond activations to construct 6H-benzo[c]chromen-6-ones

A new method for the direct ortho acyloxylation of sp2 C-H bond with various carboxylic acids was developed. A novel strategy to synthesize 6H-benzo[c]chromen-6-one derivatives was designed via Pd-catalyzed double activations of adjacent spsup