106930-04-5

Basic information

• Product Name: (2S,3R,6S)-3-Methyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran
• Synonyms: (2S,3R,6S)-3-Methyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran
• CAS NO: 106930-04-5
• Molecular Weight: 228.334
• Mol File: 106930-04-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3R,6S)-3-Methyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,6S)-3-Methyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran(106930-04-5)
• EPA Substance Registry System: (2S,3R,6S)-3-Methyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran(106930-04-5)

Safety Data

• Hazardous Substances Data: 106930-04-5(Hazardous Substances Data)

Upstream product

• 83399-62-6 (2S,3S)-3-methyl-2-phenyl-2,3-dihydro-4H-pyran-4-one 
• 100-52-7 benzaldehyde 
• 67120-85-8 (E)-1-Methoxy-3-trimethylsilyloxy-penta-1,3-dien 
• 17486-12-3 (E)-but-2-en-1-yltrimethylsilane 
• 106929-96-8 Dichloro-acetic acid (2S,3R,4R)-3-methyl-2-phenyl-3,4-dihydro-2H-pyran-4-yl ester 
• 106929-95-7 Acetic acid (2S,3R,4R)-3-methyl-2-phenyl-3,4-dihydro-2H-pyran-4-yl ester 
• 17486-13-4 (Z)-crotyltrimethylsilane 

Downstream Products

• 106930-15-8 (3S,3aR,5S,6S,7S,7aS)-3,6-Dimethyl-5-phenyl-7-phenylselanyl-hexahydro-furo[3,2-b]pyran 
• 106930-15-8 (3R,3aR,5S,6S,7S,7aS)-3,6-Dimethyl-5-phenyl-7-phenylselanyl-hexahydro-furo[3,2-b]pyran 
• 106930-14-7 (S)-2-((2S,5R,6S)-5-Methyl-6-phenyl-5,6-dihydro-2H-pyran-2-yl)-propan-1-ol 
• 106930-13-6 (R)-2-((2S,5R,6S)-5-Methyl-6-phenyl-5,6-dihydro-2H-pyran-2-yl)-propan-1-ol 
• 106930-11-4 2-((2S,5R,6S)-5-Methyl-6-phenyl-5,6-dihydro-2H-pyran-2-yl)-propionaldehyde 
• 106930-10-3 3-((2S,5R,6S)-5-Methyl-6-phenyl-5,6-dihydro-2H-pyran-2-yl)-butane-1,2-diol 

Relevant articles and documents

A Concise and Stereoselective Route to the Predominant Stereochemical Pattern of the Tetrahydropyranoid Antibiotics: An Application to Indanomycin

The reactions of (E)- and (Z)-crotylsilanes of the type R3Si-CH2-CH=CH-CH3 with activated glycal derivatives in the presence of BF3 etherate have been examined.In all cases, the reactions were regiospecific, resulting in incorporation of a 3-methylprop-1-