907195-92-0

Basic information

• Product Name: BORONIC ACID, B-[3,4-BIS[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYLPHENYL]-
• Synonyms: BORONIC ACID, B-[3,4-BIS[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYLPHENYL]-
• CAS NO: 907195-92-0
• Molecular Formula: C₁₈H₃₅BO₄Si₂
• Molecular Weight: 410.507
• Mol File: 907195-92-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BORONIC ACID, B-[3,4-BIS[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYLPHENYL]-(CAS DataBase Reference)
• NIST Chemistry Reference: BORONIC ACID, B-[3,4-BIS[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYLPHENYL]-(907195-92-0)
• EPA Substance Registry System: BORONIC ACID, B-[3,4-BIS[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYLPHENYL]-(907195-92-0)

Safety Data

• Hazardous Substances Data: 907195-92-0(Hazardous Substances Data)

Upstream product

• 1108192-19-3 ((4-bromo-1,2-phenylene)bis(oxy))bis(tert-butyldimethylsilane) 
• 2859-78-1 4-Bromoveratrole 
• 17345-77-6 1-bromo-3,4-dihydroxybenzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 1354453-73-8 8-(3'',4''-dihydroxyphenyl)-2'-deoxyguanosine 
• 907195-95-3 2-diazo-5-(3,4-di-tert-butyldimethylsilyloxyphenyl)-1-(2,4,6-trimethylphenylsulfonyl)-5-hexen-2-one 
• 907195-97-5 2-diazo-5-(3,4-dibenzoyloxyphenyl)-1-(2,4,6-trimethylphenylsulfonyl)-5-hexen-2-one 
• 907195-94-2 5-(3,4-di-tert-butyldimethylsilyloxyphenyl)-1-(2,4,6-trimethylphenylsulfonyl)-5-hexen-2-one 

Relevant articles and documents

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Hydroxyl radical-induced oxidation of a phenolic c-linked 2′-deoxyguanosine adduct yields a reactive catechol

Phenolic toxins stimulate oxidative stress and generate Clinked adducts at the C8-site of 2/-deoxyguanosine (dG). We previously reported that the C-linked adduct 8-(4″-hydroxyphenyl)-dG (p-PhOH-dG) undergoes oxidation in the presence of Na2IrCl

Asymmetric catalysis of intramolecular cyclopropanation of 5-aryl-1-diazo-1-mesitylsulfonyl-5-hexen-2-ones

We have examined the catalytic asymmetric intramolecular cyclopropanation (IMCP) reactions of 5-aryl-1-diazo-1-mesitylsulfonyl-5-hexen-2-ones, and found that the substituent of the 5-aryl group dramatically changes the enantioselectivity. That is, no enantioselectivity was observed when the substituent was a methoxy group; however, enantioselectivity was moderate when the substituent was a methylenedioxy group or a tert-butyldimethylsilyloxy group, and it dramatically increased when the substituent was lacking (96% ee) or a benzoyloxy group (93% ee).