201813-47-0

Basic information

• Product Name: Acetamide, 2,2,2-trifluoro-N-[2-[(4-methoxyphenyl)ethynyl]phenyl]-
• CAS NO: 201813-47-0
• Molecular Formula: C17H12F3NO2
• Molecular Weight: 319.283
• Mol File: 201813-47-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetamide, 2,2,2-trifluoro-N-[2-[(4-methoxyphenyl)ethynyl]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-[2-[(4-methoxyphenyl)ethynyl]phenyl]-(201813-47-0)
• EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-[2-[(4-methoxyphenyl)ethynyl]phenyl]-(201813-47-0)

Safety Data

• Hazardous Substances Data: 201813-47-0(Hazardous Substances Data)

Upstream product

• 143321-89-5 2,2,2-trifluoro-N-(2-iodophenyl)acetamide 
• 768-60-5 4-methoxyphenylacetylen 
• 615-43-0 2-iodophenylamine 
• 157869-15-3 2-((4-methoxyphenyl)ethynyl)aniline 
• 407-25-0 trifluoroacetic anhydride 

Downstream Products

• 18600-55-0 2-(4-methoxyphenyl)-4H-3,1-benzoxazin-4-one 
• 5782-11-6 2-(4-methoxyphenyl)-3-phenyl-1H-indole 
• 1233533-72-6 2-(4-methoxyphenyl)-3-(p-tolyl)-1H-indole 
• 1417732-32-1 methyl 4-(2-(4-methoxyphenyl)-1H-indol-3-yl)benzoate 
• 1385660-27-4 N-tert-butyl-2-(4-methoxyphenyl)-1H-indole-3-carboxamide 
• 1385660-50-3 N-acetyl-N-tert-butyl-2-(4-methoxyphenyl)-1H-indole-3-carboxamide 
• 1286170-00-0 C₂₀H₁₆F₃NO₂ 
• 1233533-73-7 4-(2-(4-methoxyphenyl)-1H-indol-3-yl)benzonitrile 
• 5034-76-4 indoxole 

Relevant articles and documents

Palladium-catalyzed: C -glycosylation and annulation of o -alkynylanilines with 1-iodoglycals: Convenient access to 3-indolyl- C -glycosides

An efficient and practical approach for the synthesis of 3-indolyl-C-Δ1,2-glycosides through a palladium-catalyzed annulation/C-glycosylation sequence of o-alkynylanilines with 1-iodoglycals has been developed. This methodology has a wide scope of substra

Copper-mediated cyclization-halogenation and cyclization-cyanation reactions of β-hydroxyalkynes and o -alkynylphenols and anilines

The CuX (X = I, Br, Cl, CN)-mediated cyclization-halogenation and cyclization-cyanation reactions of β-hydroxyalkynes and o-alkynylphenol and -aniline derivatives give rise to 3-halo- and 3-cyanofuro[3,2-b]pyrroles, 3-iodo-, 3-bromo-, and 3-cyanobenzofurans, and 3-cyanoindoles, respectively.