164668-41-1

Basic information

• Product Name: (5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one
• Synonyms: (5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one
• CAS NO: 164668-41-1
• Molecular Weight: 250.251
• Mol File: 164668-41-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one(164668-41-1)
• EPA Substance Registry System: (5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one(164668-41-1)

Safety Data

• Hazardous Substances Data: 164668-41-1(Hazardous Substances Data)

Upstream product

• 1006371-26-1 (5S)-5-{(R)-(tert-butyldimethylsilyloxy)-1-[(4R,5S)-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-yl]methyl}furan-2(5H)-one 
• 267660-83-3 (S)-5-((4R,5S)-5-((S)-(tert-butyldimethylsilyloxy)(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)furan-2(5H)-one 
• 252273-56-6 ethyl (2S,3R,4S)-4-hydroxy-2,3-isopropylidenedioxy-4-phenylbutanoate 
• 252273-54-4 ethyl (2S,3R,4R)-4-hydroxy-2,3-isopropylidenedioxy-4-phenylbutanoate 
• 252273-58-8 trimethyl [5S,6S,7S]-7-(t-butyldiphenylsilyloxy)-5,6-isopropylidenedioxy-4-oxo-7-phenyl-3-phenylsulfonylorthoheptanoate 
• 252273-57-7 ethyl (2S,3R,4S)-4-(t-butyldiphenylsilyloxy)-2,3-isopropylidenedioxy-4-phenylbutanoate 
• 252273-55-5 ethyl (2S,3R,4S)-2,3-isopropylidenedioxy-4-(4-nitrobenzyloxy)-4-phenylbutanoate 
• 187931-99-3 ethyl (4S,5S)-5-[(R)-{[(tert-butyl)(dimethyl)silyl]oxy}(phenyl)methyl]-2,2-dimethyl-1,3-dioxolane-4-carboxylate 
• 148162-41-8 (Z)-Methyl 4,6-O-isopropylidene-7-C-phenyl-L-ido-hept-2-enonate 

Relevant articles and documents

An expeditious enantiospecific total synthesis of (+)-7-epi-goniofufurone

Stereoselective synthesis of styryl lactone, (+)-7-epi-goniofufurone was achieved in high yield via simple transformations from tartaric acid. The key step involves the successive stereoselective reduction of ketones with borohydride and selectride. Georg

Stereoselective total synthesis of bioactive styryllactones: 9-Deoxygoniopypyrone, goniopypyrone and 7-epi-goniofufurone

Stereoselective synthesis of the bioactive styryllactones (+)-9-deoxygoniopypyrone, (+)-goniopypyrone and (+)-7-epi-goniofufurone has been achieved from D-(-)-tartaric acid. The key step involves the elaboration of a trihydroxy ester to the title compound

Enantiospecific Syntheses of (+)-Goniofufurone, (+)-7-epi-Goniofufurone, (+)-Goniobutenolide A, (-)-Goniobutenolide B, (+)-Goniopypyrone, (+)-Altholactone, (+)-Goniotriol, and (+)-7-Acetylgoniotriol

Practical and efficient syntheses of a number of styryl lactones with various structural complexities were accomplished from commercially available and inexpensive D-glycero-D-gulo-heptono-γ-lactone (D-glucoheptonic γ-lactone) (11).Lactone 11 was converte