86387-72-6

Basic information

• Product Name: phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone
• Synonyms: phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone
• CAS NO: 86387-72-6
• Molecular Weight: 416.519
• Mol File: 86387-72-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone(86387-72-6)
• EPA Substance Registry System: phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone(86387-72-6)

Safety Data

• Hazardous Substances Data: 86387-72-6(Hazardous Substances Data)

Upstream product

• 4452-11-3 1,2-diphenylprop-2-en-1-one 
• 451-40-1 phenyl benzyl ketone 
• 5431-88-9 4-benzoyltetrahydrofuran-2,3-dione 
• 3076-54-8 phenyllead(IV) triacetate 
• 107-13-1 acrylonitrile 

Downstream Products

• 115485-54-6 (5-bromo-6-methoxy-2,5,6-triphenyl-tetrahydro-pyran-2-yl)-phenyl ketone 
• 115918-32-6 (5-bromo-6-hydroxy-2,5,6-triphenyl-tetrahydro-pyran-2-yl)-phenyl ketone 
• 115035-06-8 (4-bromo-2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)-phenyl ketone 
• 107225-79-6 4,5,2'-triphenyl-spiro[furan-2,1'-indan]-3,3'-dione 
• 46878-58-4 (+/-)-3-Methylamino-1.2-diphenyl-propanon-⁽¹⁾ 
• 92646-34-9 α-aminomethyl-α'-hydroxy-bibenzyl 
• 95939-82-5 3-(5-tert-butyl-[1,3,4]thiadiazol-2-ylamino)-1,2-diphenyl-propan-1-one 
• 94864-07-0 (+/-)-3-(4-Chlor-anilino)-1.2-diphenyl-propanon-⁽¹⁾ 
• 93948-60-8 opt. inakt. 3-Isopropylamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 88783-35-1 opt. inakt. 3-Isopropylidenamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 856608-74-7 (+/-)-3-Isopropylidenamino-1.2-diphenyl-propanon-⁽¹⁾ 
• 93027-11-3 3-(N-methylamino)-1,2-diphenylpropanol 
• 92552-01-7 1,2-Diphenyl-3-iodo-1-propanone 
• 58753-66-5 (+/-)-3-Isopropylamino-1.2-diphenyl-propanon-⁽¹⁾ 

Relevant articles and documents

Catalytic Reductive Cross Coupling and Enantioselective Protonation of Olefins to Construct Remote Stereocenters for Azaarenes

A novel enantioselective protonation protocol that is triggered by reductive cross coupling of olefins is reported. When under cooperative photoredox and chiral hydrogen-bonding catalytic conditions and using a terminal reductant, various α-branched vinyl