1360109-87-0

Basic information

• Product Name: (5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-hydroxy-3-methoxyphenyl)decan-3-one
• Synonyms: (5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-hydroxy-3-methoxyphenyl)decan-3-one
• CAS NO: 1360109-87-0
• Molecular Weight: 408.654
• Mol File: 1360109-87-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-hydroxy-3-methoxyphenyl)decan-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-hydroxy-3-methoxyphenyl)decan-3-one(1360109-87-0)
• EPA Substance Registry System: (5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-hydroxy-3-methoxyphenyl)decan-3-one(1360109-87-0)

Safety Data

• Hazardous Substances Data: 1360109-87-0(Hazardous Substances Data)

Upstream product

• 69172-20-9 3-(3-methoxy-4-benzyloxyphenyl)propionaldehyde 
• 57371-44-5 3-<4-(benzyloxy)-3-methoxyphenyl>propan-1-ol 
• 1360109-85-8 C₃₀H₄₄O₄Si 
• 1360109-86-9 (S)-1-(4-(benzyloxy)-3-methoxyphenyl)-5-(tert-butyldimethylsilyloxy)dec-1-yn-3-one 
• 144735-54-6 1-ethynyl-4-(benzyloxy)-3-methoxybenzene 
• 35192-73-5 (S)-4-hydroxy-1-nonene 
• 66-25-1 hexanal 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 1360109-84-7 (S)-tert-butyldimethyl(non-1-en-4-yloxy)silane 

Downstream Products

• 1360109-90-5 (4R,6S)-4-(4-(benzyloxy)-3-methoxyphenethyl)-2,2-dimethyl-6-pentyl-1,3-dioxane 
• 1360109-92-7 (3R,5S)-1-(4-(benzyloxy)-3-methoxyphenyl)decane-3,5-diol 
• 1360109-93-8 (3R,5S)-1-(4-(benzyloxy)-3-methoxyphenyl)decane-3,5-diyl diacetate 
• 1360109-91-6 (4R,6S)-4-(3,4-dimethoxylphenetyl)-2,2-dimethyl-6-pentyl-1,3-dioxane 
• 1360109-94-9 (3R,5S)-1-(3,4-dimethoxyphenyl)decane-3,5-diol 
• 39886-76-5 [6]-gingerol 
• 863780-90-9 (3R,5S)-1-(3,4-dimethoxyphenyl)decane-3,5-diyl diacetate 
• 39886-85-6 (3S,5S)-3,5-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)decane 
• 154905-69-8 (3R,5S)-1-(4-hydroxy-3-methoxyphenyl)decane-3,5-diol 
• 53254-51-6 (3R,5S)-1-(4-hydroxy-3-methoxyphenyl)decane-3,5-diyl diacetate 

Relevant articles and documents

An Efficient Enantioselective Synthesis of Natural Gingerols, the Active Principles of Ginger

A straightforward synthesis of (S)-gingerols 1-3 has been described. The requisite stereogenic center in the target molecules was introduced by Sharpless asymmetric dihydroxylation using a chiral complex, AD-mix β. This route is simple and efficient to prepare the products in very good yields.