172995-38-9

Basic information

• Product Name: Silane, [(7-bromoheptyl)oxy](1,1-dimethylethyl)diphenyl-
• CAS NO: 172995-38-9
• Molecular Formula: C23H33BrOSi
• Molecular Weight: 433.504
• Mol File: 172995-38-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Silane, [(7-bromoheptyl)oxy](1,1-dimethylethyl)diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, [(7-bromoheptyl)oxy](1,1-dimethylethyl)diphenyl-(172995-38-9)
• EPA Substance Registry System: Silane, [(7-bromoheptyl)oxy](1,1-dimethylethyl)diphenyl-(172995-38-9)

Safety Data

• Hazardous Substances Data: 172995-38-9(Hazardous Substances Data)

Upstream product

• 10160-24-4 7-bromoheptyl alcohol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 1402548-08-6 1-(13-(tert-butyldiphenylsilyloxy)tridec-5(Z)-enyl)-3-n-pentylurea 
• 1402548-07-5 1-tert-butyldiphenylsilyloxy-13-aminotridec-8(Z)-ene 
• 1402548-06-4 1-tert-butyldiphenylsilyloxy-13-azidotridec-8(Z)-ene 
• 1184845-53-1 (Z)-13-(tert-butyldiphenylsilyloxy)tridec-5-en-1-ol 
• 1402548-05-3 13-(tert-butyldiphenylsilyloxy)tridec-5-yn-1-ol 
• 1184845-52-0 tert-butyldiphenyl(13-(tetrahydro-2H-pyran-2-yloxy)tridec-8-ynyloxy)silane 
• 170240-24-1 (10E,12R,13R)-1-tert-Butyldiphenylsilyloxy-12,13-epoxyoctadec-10-en-9-one 
• 170240-23-0 Diethyl (10-tert-butyldiphenylsilyloxy-2-oxodecyl)phosphonate 

Relevant articles and documents

Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex

A highly enantioselective synthesis of β-dimorphecolic acid 1 is reported. The synthesis features a diastereoselective reduction of the ketone 4, in which the tricarbonyliron lactone tether induces a 1,5 transfer of chirality, followed by a stereoselectiv

Synthesis of β-dimorphecolic acid exploiting highly stereoselective-reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex

A highly stereoselective synthesis of β-dimorphecolic acid is accomplished utilising a π-allyltricarbonyliron lactone complex 3 to control the formation of all the stereochemical features of the natural product.