77326-90-0

Basic information

• Product Name: 3-Butyn-1-ol, 4-[3-(trifluoromethyl)phenyl]-
• CAS NO: 77326-90-0
• Molecular Formula: C11H9F3O
• Molecular Weight: 214.187
• Mol File: 77326-90-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-Butyn-1-ol, 4-[3-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butyn-1-ol, 4-[3-(trifluoromethyl)phenyl]-(77326-90-0)
• EPA Substance Registry System: 3-Butyn-1-ol, 4-[3-(trifluoromethyl)phenyl]-(77326-90-0)

Safety Data

• Hazardous Substances Data: 77326-90-0(Hazardous Substances Data)

Upstream product

• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 927-74-2 3-Butyn-1-ol 
• 401-81-0 m-trifluoromethylphenyl iodide 
• 98-16-8 3-trifluoromethylaniline 
• 40365-61-5 2-(but-3-yn-1-yloxy)tetrahydropyran 

Downstream Products

• 77318-12-8 (Z)-4-<3-(trifluoromethyl)phenyl>-3-buten-1-ol 
• 77318-13-9 (E)-4-<3-(trifluoromethyl)phenyl>-3-buten-1-ol 
• 1352439-45-2 C₁₂H₁₀F₃NO₂ 
• 1352439-62-3 C₁₂H₈F₃NO₂ 
• 147429-92-3 1-Methyl-4-[(E)-4-(3-trifluoromethyl-phenyl)-but-3-enyl]-piperazine 
• 147429-92-3 1-Methyl-4-[(Z)-4-(3-trifluoromethyl-phenyl)-but-3-enyl]-piperazine 
• 77318-15-1 (E)-4-bromo-1-<3-(trifluoromethyl)phenyl>-1-butene 
• 77318-14-0 (Z)-4-bromo-1-<3-(trifluoromethyl)phenyl>-1-butene 

Relevant articles and documents

Accessing alternative reaction pathways of the intermolecular condensation between homo-propargyl alcohols and terminal alkynes through divergent gold catalysis

An intermolecular condensation of alkynols and terminal alkynes is reported. Using IPrAuNTf2, an efficient Au-catalyzed cyclization-alkynylation strategy furnishes (2-arylalkynyl) cyclic ethers in moderate to excellent yields (up to 94%). This strategy is extended to the synthesis of functionalized 2,3-dihydrooxepines via the sequential Au-catalyzed ring expansion of the cyclic ether substrates.

Coupling reactions of aryl bromides with 1-alkynols catalysed by a tetraphosphine/palladium catalyst

cis,cis,cis-1,2,3,4-Tetrakis(diphenylphosphinomethyl)cyclopentane/ [PdCl(C3H5)]2 system catalyses efficiently the coupling reactions of aryl halides with a variety of alkynols such as propargyl alcohol, but-1-yn-4-ol, pent