1227374-12-0

Basic information

• Product Name: (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol
• Synonyms: (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol
• CAS NO: 1227374-12-0
• Molecular Weight: 815.483
• Mol File: 1227374-12-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol(1227374-12-0)
• EPA Substance Registry System: (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol(1227374-12-0)

Safety Data

• Hazardous Substances Data: 1227374-12-0(Hazardous Substances Data)

Upstream product

• 1227373-90-1 1-(((3R,5S,7R,9S)-3,5,7,9,10-pentakis(tert-butyldimethylsilyloxy)decyloxy)methyl)-4-methoxybenzene 
• 1196989-21-5 (2S)-1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-(1,3-dithian-2-yl)propan-2-ol 
• 1196989-22-6 2-{(2S)-2-[(tert-butyldimethylsilyl)oxy]-3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-propyl}-1,3-dithiane 
• 1227373-88-7 2-((2S,4S)-2,4,5-tris(tert-butyldimethylsilyloxy)pentyl)-1,3-dithiane 
• 1227373-89-8 (R)-1-(2-((2S,4S)-2,4,5-tris(tert-butyldimethylsilyloxy)pentyl)-1,3-dithian-2-yl)-4-(4-methoxybenzyloxy)butan-2-ol 
• 101977-98-4 (S)-2,2-dimethyl-4-((S)-oxiran-2-ylmethyl)-1,3-dioxolane 
• 213978-60-0 (4R)-4-[2'-(4-methoxybenzyloxy)-ethyl]-2,2-dimethyl-[1,3]-dioxolane 
• 213978-61-1 (2R)-4-(4-methoxybenzyloxy)-butane-1,2-diol 
• 195257-62-6 (R)-2-(2-((4-methoxybenzyl)oxy)ethyl)oxirane 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1227373-79-6 (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-al 

Relevant articles and documents

C(21)-C(40) of tetrafibricin via metal catalysis: Beyond stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles

Chemical equations presented. The C(21)-C(40) fragment of fibrinogen receptor inhibitor tetrafibricin was prepared in 12 steps from propane diol (longest linear sequence). In this approach, 6 C-C bonds are formed via asymmetric iridium catalyzed transfer