110166-74-0

Basic information

• Product Name: Benzamide, 2-(1-hexynyl)-
• CAS NO: 110166-74-0
• Molecular Formula: C13H15NO
• Molecular Weight: 201.268
• Mol File: 110166-74-0.mol

Chemical Properties

• CAS DataBase Reference: Benzamide, 2-(1-hexynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 2-(1-hexynyl)-(110166-74-0)
• EPA Substance Registry System: Benzamide, 2-(1-hexynyl)-(110166-74-0)

Safety Data

• Hazardous Substances Data: 110166-74-0(Hazardous Substances Data)

Upstream product

• 693-02-7 hex-1-yne 
• 4387-36-4 2-iodobenzonitrile 
• 1885-29-6 anthranilic acid nitrile 
• 615-42-9 1,2-Diiodobenzene 
• 110166-78-4 2-(hex-1-yn-1-yl)benzonitrile 
• 4001-73-4 2-Bromobenzamide 
• 2042-37-7 o-cyanobromobenzene 
• 253435-14-2 1-iodo-2-(hex-1-ynyl)benzene 

Downstream Products

• 1192159-92-4 benzyl 2-butyl-1H-indole-1-carboxylate 
• 104919-72-4 ethyl N-[2-(1-butynyl)phenyl]carbamate 
• 1338798-01-8 12-butyl-7-phenylbenzo[c]indeno[2,1-e]azepin-5(6H)-one 

Relevant articles and documents

Highly stereoselective synthesis of (Z)-3-methoxy-1-methyleneisoindoles via DMAP catalyzed cyclization of methyl 2-alkynylbenzimidates

A DMAP (4-dimethylaminopyridine) catalyzed cyclization of methyl 2-alkynylbenzimidates has been developed, which affords 3-methoxy-1-methyleneisoindoles with excellent Z-stereoselectivity under mild and transition-metal-free conditions. The (Z)-3-methoxy-

Super acid catalysed sequential hydrolysis/cycloisomerization of o-(acetylenic)benzamides under microwave condition: Synthesis, antinociceptive and antiinflammatory activity of substituted isocoumarins

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Ruthenium-catalyzed cycloisomerization of aromatic homo- and bis-homopropargylic amines/amides: Formation of indoles, dihydroisoquinolines and dihydroquinolines

Ruthenium-catalyzed cycloisomerizations of aromatic homo- and bis-homopropargylic amines/amides efficiently afford indoles, dihydroisoquinolines and dihydroquinolines. These processes were regioselective (5- and 6-endo cyclizations) on using key Ru vinylidene intermediates. The presence of an amine/ammonium base-acid pair increased the rate of cyclization and facilitated the catalytic turnover. Copyright

A direct anionic cyclization of 2-alkynylbenzonitrile to 3- substituted-1(2H)-isoquinolones and 3-benzylideneisoindol-2ones initiated by methoxide addition

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