88596-60-5

Basic information

• Product Name: Benzenemethanol, 3-nitro-a-(phenylethynyl)-
• CAS NO: 88596-60-5
• Molecular Formula: C15H11NO3
• Molecular Weight: 253.257
• Mol File: 88596-60-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3-nitro-a-(phenylethynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3-nitro-a-(phenylethynyl)-(88596-60-5)
• EPA Substance Registry System: Benzenemethanol, 3-nitro-a-(phenylethynyl)-(88596-60-5)

Safety Data

• Hazardous Substances Data: 88596-60-5(Hazardous Substances Data)

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 536-74-3 phenylacetylene 

Downstream Products

• 1443992-31-1 4-(3-nitrophenyl)-2-phenyl-4H,5H-pyrano[3,2-c]chromen-5-one 
• 1616956-18-3 (Z)-1-(3-nitrophenyl)-3-phenylprop-2-yn-1-one O-methyl oxime 
• 31609-82-2 3-(3-nitrophenyl)-5-phenyl-1,2-oxazole 
• 1616956-28-5 4-fluoro-3-(3-nitrophenyl)-5-phenylisoxazole 
• 1183859-88-2 dimethyl 4-nitro-1-oxo-3-phenyl-1H-inden-2-ylphosphonate 
• 1315379-35-1 dimethyl 6-nitro-1-oxo-3-phenyl-1H-inden-2-ylphosphonate 
• 16616-39-0 1-(3-nitrophenyl)-3-phenylprop-2-yn-1-one 

Relevant articles and documents

Neighboring Carbonyl Group Assisted Hydration of Unsymmetrical Aryl Alkynes Overriding Regular Selectivity

A mild and highly regioselective gold-catalyzed hydration of γ-acetoxy aryl alkynes leading to anti-Markovnikov products by the assistance of a neighboring carbonyl group is presented. The reaction procedure operates under room temperature conditions with

Direct synthesis of 4-fluoroisoxazoles through gold-catalyzed cascade cyclization-fluorination of 2-alkynone O-methyl oximes

A tandem protocol for the synthesis of fluorinated isoxazoles has been developed via catalytic intramolecular cyclizations of 2-alkynone O-methyl oximes and ensuing fluorination. The reactions proceed smoothly at room temperature in the presence of 5 mol

Me3Ga-mediated alkynylation of aldehydes

The trimethylgallium reagent was found to promote the addition of phenylacetylene to various aromatic and aliphatic aldehydes. This reaction was efficiently carried out in anhydrous CH2Cl2 at room temperature under mild conditions an