326494-55-7

Basic information

• Product Name: (4S,5R)-4-(4-Methoxy-benzyloxy)-5-methyl-3-methylene-6-phenyl-hexan-1-ol
• Synonyms: (4S,5R)-4-(4-Methoxy-benzyloxy)-5-methyl-3-methylene-6-phenyl-hexan-1-ol
• CAS NO: 326494-55-7
• Molecular Weight: 340.463
• Mol File: 326494-55-7.mol

Chemical Properties

• CAS DataBase Reference: (4S,5R)-4-(4-Methoxy-benzyloxy)-5-methyl-3-methylene-6-phenyl-hexan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5R)-4-(4-Methoxy-benzyloxy)-5-methyl-3-methylene-6-phenyl-hexan-1-ol(326494-55-7)
• EPA Substance Registry System: (4S,5R)-4-(4-Methoxy-benzyloxy)-5-methyl-3-methylene-6-phenyl-hexan-1-ol(326494-55-7)

Safety Data

• Hazardous Substances Data: 326494-55-7(Hazardous Substances Data)

Upstream product

• 326494-48-8 3-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-methyl-1-phenyl-pent-4-en-1-ol 
• 326494-47-7 {2-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1-methyl-but-3-enyloxymethyl}-benzene 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 1026320-43-3 tert-butyl-{3-[1-(4-methoxy-benzyloxy)-2-methyl-3-phenyl-propyl]-but-3-enyloxy}-dimethyl-silane 
• 326494-51-3 4-benzyloxy-2-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-pent-1-en-3-ol 
• 326494-50-2 4-benzyloxy-2-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-pent-1-en-3-one 
• 159734-12-0 3-((4S,5S,6R)-2,2,5-Trimethyl-6-phenyl-[1,3]dioxan-4-yl)-but-3-en-1-ol 
• 406940-46-3 (-)-(S)-2-(benzyloxy)-N-methoxy-N-methylpropanamide 
• 154920-02-2 tert-Butyl-dimethyl-[3-((4S,5S,6R)-2,2,5-trimethyl-6-phenyl-[1,3]dioxan-4-yl)-but-3-enyloxy]-silane 
• 154920-01-1 (2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-4-methylene-1-phenyl-hexan-3-ol 
• 77287-11-7 methyl (S)-2-(benzyloxy)propanoate 

Downstream Products

• 326494-49-9 1-[(S)-4-Iodo-2-methylene-1-((R)-1-methyl-2-phenyl-ethyl)-butoxymethyl]-4-methoxy-benzene 

Relevant articles and documents

Stereoselective total synthesis of zaragozic acid A based on an acetal [1,2] Wittig rearrangement

A simultaneous creation of the C4 and C5 quaternary carbon centers by an acetal [1,2] Wittig rearrangement of O-glycoside 1 derived from L-arabino-γ-lactone is the key feature in the construction of the 2,8-dioxabicyclo[3.2.1]octane core structure of zara