1242160-39-9

Basic information

• Product Name: C₁₆H₁₃NO₄
• Synonyms: C₁₆H₁₃NO₄
• CAS NO: 1242160-39-9
• Molecular Weight: 283.284
• Mol File: 1242160-39-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₃NO₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₃NO₄(1242160-39-9)
• EPA Substance Registry System: C₁₆H₁₃NO₄(1242160-39-9)

Safety Data

• Hazardous Substances Data: 1242160-39-9(Hazardous Substances Data)

Upstream product

• 579-74-8 2-Methoxyacetophenone 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 72195-25-6 2-(2-methoxyphenyl)quinoline 
• 72195-24-5 2-(2-methoxyphenyl)quinoline 1-oxide 
• 1455213-55-4 (2’R,3’S,4’S)-1-acetyl-2’-benzoyl-4’-(2-oxo-1-(2-methoxyphenylethyl))-2-oxo-1’-tosylspiro[indoline-3,3’-tetrahydroquinoline] 

Relevant articles and documents

Cinchona-based squaramide-catalysed cascade aza-Michael-Michael addition: Enantioselective construction of functionalized spirooxindole tetrahydroquinolines

An efficient enantioselective cascade aza-Michael-Michael addition reaction catalysed by a chiral bifunctional tertiary amine-squaramide catalyst has been developed. This cascade reaction proceeded well under mild conditions, furnishing highly functionalized spirooxindole tetrahydroquinolines with three contiguous stereocenters in excellent yields with excellent diastereoselectivities (>25:1 dr) and high enantioselectivities (up to 94% ee). The Royal Society of Chemistry 2013.

Selective reduction of nitroarenes by a Hantzsch 1,4-dihydropyridine: A facile and efficient approach to substituted quinolines

An efficient reductive cyclization of o-nitrocinnamoyl compounds was achieved by employing a Hantzsch 1,4-dihydropyridine ester as a biomimetic reducing agent in the presence of catalytic palladium on carbon. This approach was successfully applied to the synthesis of substituted quinolines. Georg Thieme Verlag Stuttgart ? New York.