62056-37-5

Basic information

• Product Name: Benzene, 1-methyl-4-(3-phenyl-1-propenyl)-
• CAS NO: 62056-37-5
• Molecular Formula: C16H16
• Molecular Weight: 208.303
• Mol File: 62056-37-5.mol
• Article Data: 42

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methyl-4-(3-phenyl-1-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methyl-4-(3-phenyl-1-propenyl)-(62056-37-5)
• EPA Substance Registry System: Benzene, 1-methyl-4-(3-phenyl-1-propenyl)-(62056-37-5)

Safety Data

• Hazardous Substances Data: 62056-37-5(Hazardous Substances Data)

Upstream product

• 1586-92-1 diethyl(ethoxy)aluminum 
• 1184-58-3 dimethylaluminum chloride 
• 300-57-2 allylbenzene 
• 123726-16-9 bis(4-methylphenyl)iodonium trifluoromethanesulfonate 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 351-70-2 benzyl trifluoroacetate 
• 100-51-6 benzyl alcohol 
• 58824-48-9 1-(4-methylphenyl)-2-propen-1-ol 
• 111928-10-0 tetraphenylphosphonium trifluoromethanesulfonate 
• 98-80-6 phenylboronic acid 
• 101671-00-5 (E)-2-(4-methylphenyl)-1-nitroethene 
• 1539-57-7 diethyl 2,6-dimethyl-4-benzyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 1866-39-3 trans-p-methylcinnamic acid 
• 122058-30-4 p-methylcinnamyl alcohol 

Downstream Products

• 79542-20-4 (E)-2-phenyl-3-(p-tolyl)acrylaldehyde 
• 1452128-85-6 (E)-3-phenyl-2-(p-tolyl)acrylaldehyde 
• 1631035-62-5 1-(1-fluoro-3-phenylpropyl)-4-methylbenzene 
• 134539-88-1 2-((E)-1-Phenyl-3-p-tolyl-allyl)-2-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-malononitrile 
• 134539-89-2 2-((E)-3-Phenyl-1-p-tolyl-allyl)-2-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-malononitrile 
• 6876-68-2 N-(4-methylphenyl)-3-phenyl-2-propenamide 
• 365410-94-2 trans-N-phenyl-3-tolyl propeneamide 

Relevant articles and documents

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Starch coated magnetic nanoparticles supported palladium catalyst has been explored to perform C–C cross coupling reactions, such as oxidative Heck coupling and Tsuji–Trost allylic coupling using organosilicon compounds as one of the coupling partners. The biopolymer coated magnetic catalyst was very easy to recover magnetically and was efficiently recycled in the subsequent batches. All the reactions were performed in air and thus the necessity of air and moisture free reaction condition is avoided. The present protocols show wide substrate scope and good yields of the products.