71171-94-3

Basic information

• Product Name: Oxazole, 2-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-
• Synonyms: Oxazole, 2-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-
• CAS NO: 71171-94-3
• Molecular Formula: C₁₁H₁₂FNO
• Molecular Weight: 193.22
• Mol File: 71171-94-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 258°C at 760 mmHg
• Flash Point: 109.9°C
• Appearance: /
• Density: 1.13g/cm³
• Vapor Pressure: 0.0227mmHg at 25°C
• Refractive Index: 1.529
• CAS DataBase Reference: Oxazole, 2-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 2-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-(71171-94-3)
• EPA Substance Registry System: Oxazole, 2-(4-fluorophenyl)-4,5-dihydro-4,4-dimethyl-(71171-94-3)

Safety Data

• Hazardous Substances Data: 71171-94-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12FNO/c1-11(2)7-14-10(13-11)8-3-5-9(12)6-4-8/h3-6H,7H2,1-2H3

Upstream product

• 343316-37-0 2-(4-fluoro-benzoylamino)-2-methyl-propan-1-ol 
• 30093-99-3 4,4-dimethyl-2-oxazoline 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 129665-83-4 Li(4,4-dimethyl-2-oxazolinyl) 
• 403-43-0 4-fluorobenzoyl chloride 
• 124-68-5 2-Amino-2-methyl-1-propanol 
• 118559-32-3 4,4-dimethyl-2-(tri-n-butylstannyl)-2-oxazoline 
• 15518-10-2 3-amino-2-methyl propan-1-ol 
• 459-57-4 4-fluorobenzaldehyde 
• 104283-70-7 4,4-dimethyl-2-(4-fluorophenyl)oxazoline 
• 352-33-0 1-Chloro-4-fluorobenzene 

Downstream Products

• 166765-57-7 4-fluoro-2-nicotinoylbenzoic acid 
• 98191-74-3 2-(4-fluoro-2-methylthiophenyl)-4,4-dimethyloxazoline 
• 1619256-35-7 2-[4-fluoro-2-(2-methylallyl)phenyl]-4,4-dimethyl-1,3-oxazoline 
• 1619256-36-8 4-fluoro-2-(2-methylallyl)benzaldehyde 
• 1619256-52-8 C₂₀H₁₉FN₂ 
• 1093868-91-7 2-(2-bromo-4-fluorophenyl)-4,4-dimethyl-2-oxazoline 

Relevant articles and documents

Preparation method of acetylation intermediate of (S)-5-fluoro-3-methylisobenzofuran-3-one

The invention provides a preparation method of an acetylation intermediate of (S)-5-fluoro-3-methylisobenzofuran-3-one. The method comprises the following steps: (1) performing a reaction on a fluoroaromatic compound and a metal organic reagent to obtain

Secondary Phosphine Oxide Preligands for Palladium-Catalyzed C–H (Hetero)Arylations: Efficient Access to Pybox Ligands

C–H arylations of oxazolines were accomplished with a well-defined palladium catalyst derived from a secondary bisdiamantyl phosphine oxide. The single-component secondary phosphine oxide (SPO)-palladium complex enabled C–H activations with aryl bromides

Palladium catalyzed intramolecular acylcyanation of alkenes using α-iminonitriles

Reported here is a palladium catalyzed intramolecular acylcyanation of alkenes using α-iminonitriles. Through this method, highly functionalized indanones are synthesized in moderate to high yields using Pd(PPh 3)4, without need for any additional ligands, and a common Lewis acid (ZnCl2). Additionally, the reaction tolerates substitution at various positions on the aromatic ring including electron donating and electron withdrawing groups. This journal is the Partner Organisations 2014.