869011-52-9

Basic information

• Product Name: diethyl [3,5-bis(tert-butyldimethylsilyloxy)phenyl]methylphosphonate
• Synonyms: diethyl [3,5-bis(tert-butyldimethylsilyloxy)phenyl]methylphosphonate
• CAS NO: 869011-52-9
• Molecular Weight: 488.752
• Mol File: 869011-52-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: diethyl [3,5-bis(tert-butyldimethylsilyloxy)phenyl]methylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl [3,5-bis(tert-butyldimethylsilyloxy)phenyl]methylphosphonate(869011-52-9)
• EPA Substance Registry System: diethyl [3,5-bis(tert-butyldimethylsilyloxy)phenyl]methylphosphonate(869011-52-9)

Safety Data

• Hazardous Substances Data: 869011-52-9(Hazardous Substances Data)

Upstream product

• 187803-40-3 3,5-bis(tert-butyldimethylsilyloxy)benzaldehyde 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 103929-84-6 [3,5-di(tert-butyldimethylsilanyloxy)phenyl]methanol 
• 122-52-1 triethyl phosphite 
• 103929-83-5 methyl 3,5-bis(tert-butyldimethylsilyloxy)benzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 103929-85-7 3,5-bis(tert-butyldimethylsilyloxy)benzyl chloride 

Downstream Products

• 501-36-0 (E)-5-[2-4-(hydroxyphenyl)ethenyl]-1,3-benzenediol 
• 676596-85-3 (E)-1-(3,5-bis-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-2-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethene 

Relevant articles and documents

Resveratrol derivative containing fluorine group, and preparation method and application

The invention belongs to the technical field of medicines and discloses a resveratrol derivative containing a fluorine group, and a preparation method and an application. The resveratrol derivative has the structural characteristics as shown in a general

Biomimic transformation of resveratrol

Resveratrol was treated with several kinds of peroxidases and inorganic reagents so as to prepare ε-viniferin. Among several inorganic reagents, which were investigated in this study, thallium(III) nitrate in methanol gave (±)-ε-viniferin in the yield of 68%. On the other hand, peroxidases did not lead to ε-viniferin, but some stilbenedimers such as pallidol, resveratrol trans-dehydrodimer, and leachianol F were obtained.