114935-12-5

Basic information

• Product Name: (S)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol
• Synonyms: (S)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol
• CAS NO: 114935-12-5
• Molecular Weight: 420.624
• Mol File: 114935-12-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (S)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol(114935-12-5)
• EPA Substance Registry System: (S)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol(114935-12-5)

Safety Data

• Hazardous Substances Data: 114935-12-5(Hazardous Substances Data)

Upstream product

• 1231671-90-1 methyl (2R)-2-(benzyloxy)-3-(tert-butyldiphenylsilyloxy)propanoate 
• 114978-02-8 2,5-di-O-benzyl-1,3(R):4,6(R)-di-O-benzylidene-D-mannitol 
• 100-39-0 benzyl bromide 
• 17618-04-1 2,5-di-O-benzyl-D-mannitol 
• 544686-87-5 (S)-(-)-1-allyl-3-tert-butyldiphenylsilyl-sn-glycerol 
• 107033-46-5 (R)-(tert-butyldiphenylsilyloxy)methyloxirane 
• 100-51-6 benzyl alcohol 
• 114934-98-4 2,5-di-O-benzyl-1,6-bis-O-tert-butyldiphenylsilanyl-D-mannitol 

Downstream Products

• 1235579-81-3 1-O-(tert-butyldiphenylsilyl)-2-O-benzyl-3-O-(4,4'-dimethoxytrityl)-sn-glycerol 
• 1231671-82-1 (2R)-2-(benzyloxy)-3-(tert-butyldiphenylsilyloxy)-1-iodopropane 
• 91274-04-3 (R)-2-benzyloxy-3-trityloxy-propan-1-ol 
• 912845-78-4 [benzyloxy]-[diisopropylamino]-[2-O-benzyl-3-O-monomethoxytrityl-sn-glycero]phosphane 
• 912845-77-3 2-O-benzyl-3-O-(4-monomethoxytrityl)-sn-glycerol 
• 912845-76-2 2-O-benzyl-3-O-(4-monomethoxytrityl)-1-O-(tert-butyldiphenylsilyl)-sn-glycerol 
• 18678-94-9 2-benzyloxy-3-hexadecyloxy-1-propanol 
• 114935-16-9 2-benzyloxy-1,3-di-O-hexadecyloxy-propane 
• 114935-14-7 (R,S)-2-benzyloxy-1-tert-butyldiphenylsilanyloxy-3-hexadecyloxy-propane 
• 114935-15-8 2-benzyloxy-1,3-bis-tert-butyldiphenylsilanyloxy-propane 
• 114935-13-6 (S)-2-benzyloxy-1-tert-butyldiphenylsilanyloxy-3-trityloxy-propane 

Relevant articles and documents

Orthogonally protected glycerols and 2-aminodiols: Useful building blocks in heterocyclic chemistry

The efficient synthesis of orthogonally protected glycerols, 2-aminopropane-1,3-diols and 2-aminobutane-1,4-diols that can constitute useful tools in heterocyclic chemistry, is reported. These interesting tri-functionalized small synthons were easily prepared from serine or aspartic acid. In addition, these substrates can be readily transformed into their iodide derivatives in very good yields. ARKAT USA, Inc.

A Staphylococcus aureus lipoteichoic acid (LTA) derived structural variant with two diacylglycerol residues

Based on 1,2-O-isopropylidene-sn-glycerol five chiral building blocks containing differently modified glycerol residues were required for the synthesis of the target molecule 2. One of these building blocks is diacylglyceryl β-gentiobioside carrying a pho

Platelet activating factor. Synthetic studies

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