885118-01-4

Basic information

• Product Name: (S)-6-[(4-benzyloxy)phenethyl]-5,6-dihydropyran-2-one
• Synonyms: (S)-6-[(4-benzyloxy)phenethyl]-5,6-dihydropyran-2-one
• CAS NO: 885118-01-4
• Molecular Weight: 308.377
• Mol File: 885118-01-4.mol

Chemical Properties

• CAS DataBase Reference: (S)-6-[(4-benzyloxy)phenethyl]-5,6-dihydropyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-6-[(4-benzyloxy)phenethyl]-5,6-dihydropyran-2-one(885118-01-4)
• EPA Substance Registry System: (S)-6-[(4-benzyloxy)phenethyl]-5,6-dihydropyran-2-one(885118-01-4)

Safety Data

• Hazardous Substances Data: 885118-01-4(Hazardous Substances Data)

Upstream product

• 850251-79-5 (S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-yl acrylate 
• 850251-73-9 1-(4-(benzyloxy)phenyl)hex-5-en-3-ol 
• 68486-77-1 3-(4-(benzyloxy)phenyl)propanal 
• 100-39-0 benzyl bromide 
• 10210-17-0 3-(4-hydroxyphenyl)propan-1-ol 
• 61440-45-7 3-[4-(benzyloxy)phenyl]propan-1-ol 
• 871809-93-7 (+)-(3R)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 
• 767330-04-1 (-)-(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 

Downstream Products

• 30358-99-7 Centrolobin 
• 885118-13-8 (4R,6S)-6-[2-(4-Benzyloxy-phenyl)-ethyl]-4-(4-methoxy-2,6-bis-methoxymethoxy-phenyl)-tetrahydro-pyran-2-one 
• 885118-10-5 (S)-6-[2-(4-Benzyloxy-phenyl)-ethyl]-4-(4-methoxy-2,6-bis-methoxymethoxy-phenyl)-5,6-dihydro-pyran-2-one 
• 885118-12-7 (4R,6S)-6-[2-(4-Hydroxy-phenyl)-ethyl]-4-(4-methoxy-2,6-bis-methoxymethoxy-phenyl)-tetrahydro-pyran-2-one 
• 885118-11-6 (S)-6-[2-(4-Hydroxy-phenyl)-ethyl]-4-(4-methoxy-2,6-bis-methoxymethoxy-phenyl)-5,6-dihydro-pyran-2-one 
• 885117-99-7 trifluoro-methanesulfonic acid 2-[2-(4-benzyloxy-phenyl)-ethyl]-6-oxo-3,6-dihydro-2H-pyran-4-yl ester 
• 885118-05-8 (S)-6-[2-(4-Benzyloxy-phenyl)-ethyl]-dihydro-pyran-2,4-dione 
• 885118-04-7 (4S,6S)-6-[2-(4-Benzyloxy-phenyl)-ethyl]-4-hydroxy-tetrahydro-pyran-2-one 
• 767330-06-3 (R)-6-(4-hydroxyphenethyl)tetrahydropyran-2-one 

Relevant articles and documents

Lipase-catalyzed resolution of 1-[4-(benzyloxy)phenyl]hex-5-en-3-ol: Synthesis of (-)-centrolobine

A practical and efficient method for the preparation of homoallylic alcohol and its successful enzymatic resolution has been developed. This lipase-catalyzed resolution process has been optimized with respect to different lipases and solvents. Moreover, M

Total synthesis of (-)-centrolobine: β-C-glycoside formation via a tandem Grignard addition and stereoselective hemi-ketal reduction

It has been demonstrated that an aryl-β-C-glycoside can be efficiently constructed via a sequence consisting of Brown asymmetric allylation, ring-closing metathesis, hydrogenation, nucleophilic addition, and stereoselective Et3SiH reduction. Th