60901-21-5

Basic information

• Product Name: Benzoic acid, 2-(2-phenylethenyl)-
• CAS NO: 60901-21-5
• Molecular Formula: C15H12O2
• Molecular Weight: 224.259
• Mol File: 60901-21-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-(2-phenylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-(2-phenylethenyl)-(60901-21-5)
• EPA Substance Registry System: Benzoic acid, 2-(2-phenylethenyl)-(60901-21-5)

Safety Data

• Hazardous Substances Data: 60901-21-5(Hazardous Substances Data)

Upstream product

• 7011-98-5 3-benzyl-3H-isobenzofuran-1-one 
• 2674-44-4 3-phenyl-isochroman-1-one 
• 87717-18-8 Ethyl 2-(2-phenylethenyl)benzoate 
• 100-42-5 styrene 
• 88-67-5 2-Iodobenzoic acid 
• 63104-88-1 Methyl 2-styrylbenzoate 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 7677-24-9 trimethylsilyl cyanide 
• 62-53-3 aniline 
• 119-67-5 o-carboxybenzaldehyde 
• 14783-89-2 ortho-carboxybenzenediazonium tetrafluoroborate 
• 6091-64-1 2-bromobenzoic acid ethyl ester 

Downstream Products

• 2674-44-4 3-phenyl-isochroman-1-one 
• 92424-73-2 3-(nitro-phenyl-methylene)-3H-isobenzofuran-1-one 
• 106477-49-0 α,α'-dibromo-bibenzyl-2-carboxylic acid 
• 4393-04-8 2-styryl-benzyl alcohol 
• 204847-93-8 trans-stilbene-2-carbonyl chloride 
• 118-90-1 ortho-methylbenzoic acid 
• 65-85-0 benzoic acid 
• 21868-93-9 2,3-Diphenyl-3,4-dihydro-isocarbostyril 
• 4679-90-7 3-benzyl-N-phenyl isoindolin-1-one 
• 86770-01-6 (E)-N-(tert-butyl)-2-styrylbenzamide 
• 86769-97-3 (E)-N-methyl-2-styrylbenzamide 
• 39142-92-2 N,9-dibenzyl-8-azabicyclo<4.3.0>nona-1(6),2,4-trien-7-one 
• 86770-02-7 3-Benzyl-2,3-dihydro-2-methyl-1H-isoindol-1-one 
• 39142-91-1 3-benzyl-2,3-dihydro-1H-isoindolin-1-one 

Relevant articles and documents

Synthesis and characterization of mesoporous organosilica supported palladium (SBA-Pr-NCQ-Pd) as an efficient nanocatalyst in the Mizoroki–Heck coupling reaction

In the present study, the modification of a mesoporous organosilica nanocomposite SBA-15 (Santa Barbara Amorphous 15) was carried out in two steps, first through the surface functionalization of SBA-Pr-NH2 with 2-chloroquinoline-3-carbaldehyde to form SBA-Pr-NCQ, and then through a post-modification process with palladium ions. The target nanocompound structure of SBA-Pr-NCQ-Pd was characterized by different techniques (thermogravimetric analysis, X-ray diffraction, scanning electron microscopy, Energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy). The catalytic performance of the porous inorganic–organic hybrid nanocomposite (SBA-Pr-NCQ-Pd) in one of the most important carbon–carbon bond-forming processes, the Mizoroki–Heck coupling reaction of aryl halides and methacrylate in water/ethanol media, was examined. Compared to previous reports, this protocol afforded some advantages, such as high yields of products, short reaction times, catalyst stability without leaching, simple methodology, easy workup, and greener conditions. Also, the nanocatalyst can be easily separated from the reaction mixture and reused several times without a significant decrease in activity and promises economic as well as environmental benefits.

A facile and efficient method for the synthesis of N-substituted 3-oxoisoindoline-1-carbonitrile derivatives catalyzed by sulfamic acid

A new and efficient method for the synthesis of N-substituted 3-oxoisoindoline-1-carbonitrile derivatives by a one-pot, three-component condensation reaction of 2-carboxybenzaldehyde, primary amine, and TMSCN in the presence of 10 mol % sulfamic acid (NH2SO3H) as the catalyst in EtOH under reflux temperature is described. The process is simple and environmentally benign and the catalyst is commercially available and inexpensive. ARKAT-USA, Inc.

Benzamidoaldehydes and their use as cysteine protease inhibitors

Compounds of the formula where R1, R2, R3, X and n are as defined in the description, are inhibitors of cysteine protease.