173901-21-8

Basic information

• Product Name: 4-(2-(tert-butyldimethylsilyloxy)ethyl)benzenamine
• Synonyms: 4-(2-(tert-butyldimethylsilyloxy)ethyl)benzenamine
• CAS NO: 173901-21-8
• Molecular Weight: 251.444
• Mol File: 173901-21-8.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 4-(2-(tert-butyldimethylsilyloxy)ethyl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-(tert-butyldimethylsilyloxy)ethyl)benzenamine(173901-21-8)
• EPA Substance Registry System: 4-(2-(tert-butyldimethylsilyloxy)ethyl)benzenamine(173901-21-8)

Safety Data

• Hazardous Substances Data: 173901-21-8(Hazardous Substances Data)

Upstream product

• 100-27-6 2-(4-nitrophenyl)ethanol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 288-32-4 1H-imidazole 
• 104-10-9 2-(4'-aminophenyl)ethyl alcohol 

Downstream Products

• 949495-48-1 ethyl ({4-[2-(tert-butyldimethylsilyloxy)ethyl]phenyl}amino)(oxo)acetate 
• 949495-50-5 ethyl {[4-(2-hydroxyethyl)phenyl]amino}(oxo)acetate 
• 949495-56-1 ethyl 7-[2-(4-{[ethoxy(oxo)acetyl]amino}phenyl)ethoxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate 
• 949495-62-9 ethyl ({4-[2-({5-hydroxy-2-[(4-methoxybenzylamino)carbonyl]-4-oxo-4H-chromen-7-yl}oxy)ethyl]phenyl}amino)(oxo)acetate 
• 408369-69-7 N-[4-(2-{(tert-butyl(dimethyl)silyl]oxy}ethyl)phenyl]-4'-(trifluoromethyl)-1,1'-biphenyl-2-carboxamide 
• 246219-85-2 N-(4-(2-((tert-butyldimethylsilyl)oxy)ethyl)phenyl)methanesulfonamide 

Relevant articles and documents

High-Throughput Immunochemical Method to Assess the 2-Heptyl-4-quinolone Quorum Sensing Molecule as a Potential Biomarker of Pseudomonas aeruginosa Infections

Bacterial quorum sensing (QS) is being contemplated as a promising target for developing innovative diagnostic and therapeutic strategies. Here we report for the first time the development of antibodies against 2-heptyl-4-quinolone (HHQ), a signaling mole

BIFUNCTIONAL COMPOUNDS

The invention provides a bifunctional compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein said Targeting Ligand, Linker and Degron are as described herein.

Palladium-catalyzed amination of aryl chlorides and bromides with ammonium salts

We report the palladium-catalyzed coupling of aryl halides with ammonia and gaseous amines as their ammonium salts. The coupling of aryl chlorides and ortho-substituted aryl bromides with ammonium sulfate forms anilines with higher selectivity for the primary arylamine over the diarylamine than couplings with ammonia in dioxane. The resting state for the reactions of aryl chlorides is different from the resting state for the reactions of aryl bromides, and this change in resting states is proposed to account for a difference in selectivities for reactions of the two haloarenes.