113984-68-2

Basic information

• Product Name: TERT-BUTYL(4-FLUOROPHENOXY)DIMETHYLSILANE
• Synonyms: TERT-BUTYL(4-FLUOROPHENOXY)DIMETHYLSILANE;Benzene, 1-[[(1,1-diMethylethyl)diMethylsilyl]oxy]-4-fluoro-;Tert-Butyl(4-Fluorophenoxy)Dimethylsilane(WX635004)
• CAS NO: 113984-68-2
• Molecular Formula: C₁₂H₁₉FOSi
• Molecular Weight: 226.3625632
• Mol File: 113984-68-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TERT-BUTYL(4-FLUOROPHENOXY)DIMETHYLSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: TERT-BUTYL(4-FLUOROPHENOXY)DIMETHYLSILANE(113984-68-2)
• EPA Substance Registry System: TERT-BUTYL(4-FLUOROPHENOXY)DIMETHYLSILANE(113984-68-2)

Safety Data

• Hazardous Substances Data: 113984-68-2(Hazardous Substances Data)

Upstream product

• 371-41-5 4-Fluorophenol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 113984-67-1 5-((tert-butyldimethylsilyl)oxy)-2-fluorobenzaldehyde 
• 72358-73-7 (4-fluorophenyl) benzenesulfonate 
• 873426-76-7 tert-butyldimethylsilyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl ether 
• 405-51-6 4-fluorophenyl acetate 
• 132362-07-3 (5,7-Bis-benzyloxy-4-fluoro-1H-indol-3-ylmethyl)-trimethyl-ammonium; iodide 
• 132303-37-8 5,7-Bis-benzyloxy-4-fluoro-1H-indole-2-carboxylic acid methyl ester 
• 132303-50-5 (5,7-Bis-benzyloxy-4-fluoro-1H-indol-3-yl)-acetonitrile 
• 132303-40-3 5,7-Bis-benzyloxy-4-fluoro-1H-indole-2-carbaldehyde 
• 132303-53-8 2-(5,7-Bis-benzyloxy-4-fluoro-1H-indol-3-yl)-ethylamine 
• 132303-46-9 (5,7-Bis-benzyloxy-4-fluoro-1H-indol-3-ylmethyl)-dimethyl-amine 
• 132303-43-6 5,7-Bis-benzyloxy-4-fluoro-1H-indole 
• 113984-71-7 2-fluoro-3,5-dimethoxy-benzaldehyde 
• 113984-72-8 3,5-Bis-benzyloxy-2-fluoro-benzaldehyde 
• 103439-07-2 6-fluorophenylephrine 

Relevant articles and documents

COMPOUNDS AND COMPOSITIONS FOR USE IN TREATING SKIN DISORDERS

Provided herein is a compound of formula (XXXII) or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer thereof or a physiologically functional derivative thereof, wherein R1, R2, R3, G, A, E, n, p, and q are defined herein. Also provided herein are compositions comprising a compound of formula (XXXII), and methods of using a compound of formula (XXXII), e.g., in the treatment or prevention of skin disorders.

The effect of solvent accessible surface on Hammett-type dependencies of infinite dilution 29Si and 13C NMR shifts in ring substituted silylated phenols dissolved in chloroform and acetone

Infinite dilution 29Si and 13C NMR chemical shifts were determined from concentration dependencies of the shifts in dilute chloroform and acetone solutions of para substituted O-silylated phenols, 4-R-C6H4-O-SiR′2R″ (R = Me, MeO, H, F, Cl, NMe2, NH2, and CF3), where the silyl part included groups of different sizes: dimethylsilyl (R′ = Me, R″ = H), trimethylsilyl (R′ = R″ = Me), tert-butyldimethylsilyl (R′ = Me, R″ = CMe3), and tert-butyldiphenylsilyl (R′ = C6H5, R″ = CMe3). Dependencies of silicon and C-1 carbon chemical shifts on Hammett substituent constants are discussed. It is shown that the substituent sensitivity of these chemical shifts is reduced by association with chloroform, the reduction being proportional to the solvent accessible surface of the oxygen atom in the Si-O-C link. Copyright

Dose-dependent antithrombotic activity of an orally active tissue factor/factor VIIa inhibitor without concomitant enhancement of bleeding propensity

The discovery of a highly potent and selective tissue factor/factor VIIa inhibitor is described. Upon oral administration of its double prodrug in the guinea pig, a dose-dependent antithrombotic effect is observed in an established model of arterial throm