7217-41-6

Basic information

• Product Name: Silane, (3-fluorophenyl)trimethyl-
• CAS NO: 7217-41-6
• Molecular Formula: C9H13FSi
• Molecular Weight: 168.286
• Mol File: 7217-41-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Silane, (3-fluorophenyl)trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, (3-fluorophenyl)trimethyl-(7217-41-6)
• EPA Substance Registry System: Silane, (3-fluorophenyl)trimethyl-(7217-41-6)

Safety Data

• Hazardous Substances Data: 7217-41-6(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 1073-06-9 3-fluorobromobenzene 
• 625-98-9 3-chlorofluorobenzene 
• 128254-27-3 2-Fluoro-1,4-bis-trimethylsilanyl-benzene 

Downstream Products

• 345-83-5 4-fluorobenzophenone 
• 345-69-7 3-fluorobenzophenone 
• 701-27-9 3-fluorobenzene-1-sulfonyl chloride 
• 1121-86-4 1-Fluoro-3-iodobenzene 
• 1524-40-9 3-fluorobenzenesulfonyl amide 
• 462-06-6 fluorobenzene 
• 1234714-98-7 C₂₀H₂₀FNO₃ 
• 130043-78-6 Sodium; 3-fluoro-benzenesulfonate 
• 34557-54-5 methane 
• 41866-81-3 trimethylsiloxide anion 
• 62476-44-2 3-Fluor-1,4-dihydrotrimethylsilylbenzol 
• 455-36-7 1-(3-fluorophenyl)ethanone 
• 128254-29-5 (2-Fluoro-4-trimethylsilanyl-phenyl)-phenyl-methanone 
• 130043-77-5 1-(3-Fluoro-phenyl)-3-methyl-but-2-en-1-one 

Relevant articles and documents

Generation of Aryllithium Reagents from N -Arylpyrroles Using Lithium

Treatment of 1-aryl-2,5-diphenylpyrroles with lithium powder in tetrahydrofuran at 0 °C results in the generation of the corresponding aryllithium reagents through reductive C-N bond cleavage.

Arylsilanes: Application to gold-catalyzed oxyarylation of alkenes

Arylsilanes are efficient reagents for the gold-catalyzed oxyarylation of alkenes (21 examples, up to 85% isolated yield). Using commercially available Ph3PAuCl and readily prepared, benign arylsilanes, these two- and three-component reactions

UNE VOIE ORIGINALE ET SELECTIVE DE FONCTIONNALISATION EN POSITION META DU FLUORO- ET DE L'ETHYLBENZENE

An original and regioselective method for the meta functionalisation of fluoro- and ethylbenze is reported.This process involves a 2,5-disilylation of these subtrates using trimethylchlorosilane in the presence of lithium in THF as the solvent.After aromatisation, monodesilylation in position 2- and electrophilic substitution of the trimethylsilyl group in position 5-, meta acetyl-, senecioyl-, benzoyl-, and iodofluorobenzenes and ethylbenzenes as well as the sodium salts of metafluoro or meta ethylbenzenesulfonic acid and 3-aminosulfonylfluorobenzene were obtained in good yields. pair of diastereomeric triamines 15 and 16.A tricyclic diazasystem 19 was formed from the reaction of cyanide with the carbamoylated chloroenamine 18.Monochloroenamine 10a and dichloroenamine 12a showed a significant mutagenic behaviour in the Ames test.