56700-87-9

Basic information

• Product Name: 4-[3-Methoxy-4-[(trimethylsilyl)oxy]phenyl]-2-butanone
• Synonyms: 4-[3-Methoxy-4-[(trimethylsilyl)oxy]phenyl]-2-butanone
• CAS NO: 56700-87-9
• Molecular Formula: C₁₄H₂₂O₃Si
• Molecular Weight: 266.41
• Mol File: 56700-87-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 322.7±37.0 °C(Predicted)
• Appearance: /
• Density: 0.989±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-[3-Methoxy-4-[(trimethylsilyl)oxy]phenyl]-2-butanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[3-Methoxy-4-[(trimethylsilyl)oxy]phenyl]-2-butanone(56700-87-9)
• EPA Substance Registry System: 4-[3-Methoxy-4-[(trimethylsilyl)oxy]phenyl]-2-butanone(56700-87-9)

Safety Data

• Hazardous Substances Data: 56700-87-9(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 122-48-5 4-(4-hydroxy-3-methoxyphenyl)-2-butanone 
• 121-33-5 vanillin 
• 1080-12-2 (E)-4-(4-hydroxy-3-methoxyphenyl)but-3-ene-2-one 

Downstream Products

• 77333-94-9 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)tridecan-3-one 
• 107257-18-1 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)tetradecan-3-one 
• 77333-93-8 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)undecan-3-one 
• 77398-91-5 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)nonan-3-one 
• 77398-92-6 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dodecan-3-one 
• 122-48-5 4-(4-hydroxy-3-methoxyphenyl)-2-butanone 
• 39728-80-8 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)butane 
• 77333-91-6 4-hydroxy-3-(4-hydroxy-3-methoxybenzyl)nonan-2-one 
• 23513-14-6 (+/-)-[6]-gingerol 
• 1035798-55-0 C₂₀H₃₄O₄Si 
• 1360874-94-7 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-phenylhexan-3-one 
• 1360874-98-1 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-11-phenylundecan-3-one 
• 23513-13-5 [6]-shogaol 
• 61871-71-4 1-(4-hydroxy-3-methoxyphenyl)decane-3,5-dione 

Relevant articles and documents

Syntheses of the (+/-)--Gingerols (Pungent Principles of Ginger) and Related Compounds through Regioselective Aldol Condensations: Relative Pungency Assays

The deprotonation of trimethylsilylzingerone (13) by lithium di-isopropylamide at -78 deg C has been found to be regioselective (92 : 8 in favour of less-substituted enolate): the anion was condensed with alkanals and acyl imidazoles to give convenient syntheses of (+/-)--- and --gingerols (1) and -, -, and -gingerdiones (9).Similary, 3-methoxy-4-trimethylsilyloxybenzylideneacetone (17) gave the (+/-)---dehydrogingerols (8) and -, -, and -dehydrogingerdiones (10).The aldol reaction to -gingerol and methyl -gingerol was also conducted through a vinyloxyborane or through the enol silyl ether (TiCl4 catalysis).Results of organoleptic assays on these compounds are discussed, and the relation between pungency in the gingerols and in capsaicin is commented on.The aldol method was also used to synthesise the natural β-ketols(+/-)-daphneolone (25) and (+/-)-hexahydrocurcumin (4).