13335-50-7

Basic information

• Product Name: Benzene, 2-methoxy-1-(phenylmethoxy)-4-propyl-
• CAS NO: 13335-50-7
• Molecular Formula: C17H20O2
• Molecular Weight: 256.345
• Mol File: 13335-50-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 2-methoxy-1-(phenylmethoxy)-4-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-methoxy-1-(phenylmethoxy)-4-propyl-(13335-50-7)
• EPA Substance Registry System: Benzene, 2-methoxy-1-(phenylmethoxy)-4-propyl-(13335-50-7)

Safety Data

• Hazardous Substances Data: 13335-50-7(Hazardous Substances Data)

Upstream product

• 120-11-6 2-methoxy-1-(phenylmethoxy)-4-(1-propenyl)-benzene 
• 57371-42-3 4-allyl-1-benzyloxy-2-methoxybenzene 
• 2785-87-7 2-methoxy-4-n-propylphenol 
• 100-44-7 benzyl chloride 

Downstream Products

• 2785-87-7 2-methoxy-4-n-propylphenol 

Relevant articles and documents

Generation of Hydrogen from Water: A Pd-Catalyzed Reduction of Water Using Diboron Reagent at Ambient Conditions

Production of hydrogen from renewable sources, particularly from water, is an intensive area of research, which has far-reaching relevance in hydrogen economy. A homogeneous catalytic method is presented for producing clean hydrogen gas from water, in a reaction of water with a diboron compound as the reductant, under ambient reaction conditions. The Pd-catalytic system is stable in water and displays excellent recyclability. Hydroxy analogues such as alcohols are compatible with the Pd/B2Pin2 system and generate hydrogen gas efficiently. The B2Pin2-H2O system, in the presence of palladium, is an excellent catalytic system for selective hydrogenation of olefins.

Development of a palladium on boron nitride catalyst and its application to the semihydrogenation of alkynes

The simple preparative method for a novel palladium supported on boron nitride catalyst (Pd/BN) was accomplished. Pd/BN is widely applicable for the semihydrogenation of mono- as well as disubstituted alkynes to furnish the corresponding alkenes in the presence of diethylenetriamine (DETA), which exhibits both an unprecedented acceleration effect toward the semihydrogenation and a suppression effect with regard to the overhydrogenation to alkanes. Copyright

Development of molecular sieves-supported palladium catalyst and chemoselective hydrogenation of unsaturated bonds in the presence of nitro groups

The chemoselective hydrogenation of unsaturated bonds and azide functionalities is achieved in the presence of nitro groups by a heterogeneous palladium catalyst supported on molecular sieves (MS3A). The present method shows a widerange of applicability with regard to substrates and the catalyst can be easily prepared and reused at least three times without any loss of activity.