1239481-06-1

Upstream product

• 1239481-05-0 2-(4-(azidomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 536-74-3 phenylacetylene 
• 138500-85-3 4-bromomethylphenylboronic acid pinacol ester 

Downstream Products

• 1239481-16-3 4-phenyl-1-(4-(thiophen-2-yl)benzyl)-1,2,3-triazole 
• 1239481-15-2 3-(4-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)phenyl)pyridine 
• 1239481-14-1 1-((4'-methoxybiphenyl-4-yl)methyl)-4-phenyl-1,2,3-triazole 
• 1239481-12-9 1-((4'-methylbiphenyl-4-yl)methyl)-4-phenyl-1,2,3-triazole 
• 1239481-13-0 1-((2'-methylbiphenyl-4-yl)methyl)-4-phenyl-1,2,3-triazole 

Relevant academic research and scientific papers

LOW PRESSURE NANOWIRE MEMBRANE FOR CATALYTIC REACTIONS AND METHODS OF MAKING AND USING THE SAME

In embodiments a metal or metal alloy nanowires are assembled into a nanoporous membrane that can be used in methods for catalyzing various reactions under low pressures and achieving high flow rate of the reactions. In embodiments, the membranes of the d

INHIBITORS OF FATTY ACID AMIDE HYDROLASE

The present invention provides compounds, and pharmaceutically acceptable compositions thereof, encompassed by any of formulae (I), (II), (III), (IV), (V), or (VI), or subgenera thereof. The present invention also provides methods for treating an FAAH mediated disease, disorder or condition by administering a therapeutically effective amount of a compound or composition comprising a compound of any of formulae (I), (II), (III), (IV), (V), or (VI), or subgenera thereof, to a patient in need thereof. Additionally, the present invention provides methods for inhibiting FAAH by administering a therapeutically effective amount of a compound or composition comprising a compound of any of formulae (I), (II), (III), (IV), (V), or (VI), or subgenera thereof, to a patient in need thereof.

A modular approach to catalytic synthesis using a dual-functional linker for Click and Suzuki coupling reactions

The stable benzylazido-boronate ester 1 is presented as an example of a dual-functional linker that allows the synthetically valuable boronate motif to be clicked onto other molecules under mild conditions. The utility of the azido-boronate motif as a modular building block is demonstrated in the rapid synthesis of drug-like structures employing sequential catalytic azide-alkyne cycloaddition and Suzuki coupling reactions.