1172102-18-9

Basic information

• Product Name: (3S,5S)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol
• Synonyms: (3S,5S)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol
• CAS NO: 1172102-18-9
• Molecular Weight: 300.398
• Mol File: 1172102-18-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (3S,5S)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,5S)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol(1172102-18-9)
• EPA Substance Registry System: (3S,5S)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol(1172102-18-9)

Safety Data

• Hazardous Substances Data: 1172102-18-9(Hazardous Substances Data)

Upstream product

• 1172102-05-4 4-[(3S,5S)-3-hydroxy-5-tert-butyldiphenylsilanyloxy-7-phenylheptyl]phenol 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 87030-11-3 ethyl 3-(4-(benzyloxy)phenyl)acrylate 
• 61440-45-7 3-[4-(benzyloxy)phenyl]propan-1-ol 
• 1428899-28-8 (4R,6S)-2,2-dimethyl-6-{2-[4-(phenylmethoxy)phenyl]ethyl}-1,3-dioxan-4-carboxaldehyde 
• 1428899-26-6 (4R,6S)-2,2-dimethyl-4-[(1E)-2-phenylethenyl]-6-{2-[4-(phenylmethoxy)phenyl]ethyl}-1,3-dioxane 
• 1428899-25-5 (4R,6S)-2,2-dimethyl-6-{2-[4-(phenylmethoxy)phenyl]ethyl}-1,3-dioxan-4-methanol 
• 1428899-14-2 (4S,6R)-4-{[(4-methoxyphenyl)methoxy]methyl}-2,2-dimethyl-6-{2-[4-(phenylmethoxy)phenyl]ethyl}-1,3-dioxane 
• 1428899-19-7 (2S,4R)-1-[(4-methoxyphenyl)methoxy]-6-[4-(phenylmethoxy)phenyl]hexane-2,4-diol 
• 1428899-17-5 (1R)-1-{(2R,3R)-3-{[(4-methoxyphenyl)methoxy]methyl}oxiran-2-yl}-3-[4-(phenylmethoxy)phenyl]propan-1-ol 
• 1428899-18-6 (3R)-6-[(4-methoxyphenyl)methoxy]-1-[4-(phenylmethoxy)phenyl]hex-4-en-3-ol 
• 123-08-0 4-hydroxy-benzaldehyde 
• 1428899-15-3 6-[(4-methoxyphenyl)methoxy]-1-[4-(phenylmethoxy)phenyl]hex-4-en-3-ol 
• 1428899-16-4 6-[(4-methoxyphenyl)methoxy]-1-[4-(phenylmethoxy)phenyl]hex-4-yn-3-ol 

Relevant articles and documents

The first stereoselective total synthesis of naturally occurring, bioactive (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol and the synthesis of its enantiomer

The first stereoselective total synthesis of the naturally occurring anti-emetic diarylheptanoid (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol (1) was accomplished starting from 4-hydroxybenzaldehyde and involving a Sharpless kinetic resolution and

Chiron approach to the synthesis of yashabushidiol B, (3S,5S)-1-(4′- hydroxyphenyl)-7-phenylheptane-3,5-diol, and its 4′-methoxy analogue

The total synthesis of yashabushidiol B 4, a linear diarylheptanoid containing a 1,3-diol system and its analogues 5 and 6 has been achieved by utilizing intermediate 7, which was derived from d-glucose. The Wittig reaction is the key step of our syntheti