10366-86-6

Basic information

• Product Name: Benzamide, N,N-diethyl-3-fluoro-
• CAS NO: 10366-86-6
• Molecular Formula: C11H14FNO
• Molecular Weight: 195.237
• Mol File: 10366-86-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N,N-diethyl-3-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N,N-diethyl-3-fluoro-(10366-86-6)
• EPA Substance Registry System: Benzamide, N,N-diethyl-3-fluoro-(10366-86-6)

Safety Data

• Hazardous Substances Data: 10366-86-6(Hazardous Substances Data)

Upstream product

• 109-89-7 diethylamine 
• 1711-07-5 3-fluorobenzoyl chloride 
• 401-77-4 3-fluoro-1-(trichloromethyl)benzene 
• 121-44-8 triethylamine 

Downstream Products

• 150079-44-0 N,N-Diethyl-2-chloro-3-fluorobenzamide 
• 1620210-48-1 N,N-diethyl-3-fluoro-2-(1-phenylethyl)benzamide 
• 1620210-54-9 N,N-diethyl-5-fluoro-2-(1-phenylethyl)benzamide 
• 121425-03-4 N,N-diethyl-3-fluoro-6-formyl-2-(trimethylsilyl)benzamide 
• 121425-02-3 N,N-diethyl-3-fluoro-6-methyl-2-(trimethylsilyl)benzamide 
• 121425-10-3 N,N-diethyl-6-deuterio-3-fluorobenzamide 
• 121425-11-4 N,N-diethyl-5-fluoro-2-methylbenzamide 
• 143024-53-7 4-fluoro-3-phenyl-2-benzofuran-1(3H)-one 
• 121424-94-0 N,N-diethyl-3-fluoro-2-(trimethylsilyl)benzamide 
• 15789-04-5 N,N-diethyl-3-hydroxybenzamide 
• 1383479-33-1 C₃₀H₃₄N₂O₄ 

Relevant articles and documents

One-Pot Synthesis of Tertiary Amides from Organic Trichlorides through Oxygen Atom Incorporation from Air by Convergent Paired Electrolysis

A convergent paired electrolysis catalyzed by a B12 complex for the one-pot synthesis of a tertiary amide from organic trichlorides (R-CCl3) has been developed. Various readily available organic trichlorides, such as benzotrichloride and its derivatives, chloroform, dichlorodiphenyltrichloroethane (DDT), trichloro-2,2,2-trifluoroethane (CFC-113a), and trichloroacetonitrile (CNCCl3), were converted to amides in the presence of tertiary amines through oxygen incorporation from air at room temperature. The amide formation mechanism in the paired electrolysis, which was mediated by a cobalt complex, was proposed.

Branch-selective, Iridium-catalyzed hydroarylation of monosubstituted alkenes via a cooperative destabilization strategy

Highly branch-selective, carbonyl-directed hydroarylations of monosubstituted alkenes are described. The chemistry relies upon a cationic Ir(I) catalyst modified with an electron deficient, wide bite angle bisphosphine ligand. This work provides a regioisomeric alternative to the Murai hydroarylation protocol.