16728-57-7

Upstream product

• 22921-72-8 (5-bromopentoxy)benzene 
• 151-50-8 potassium cyanide 
• 6628-78-0 6-chlorohexanenitrile 
• 139-02-6 sodium phenoxide 
• 40339-97-7 (5-iodo-pentyl)-phenyl ether 
• 143-33-9 sodium cyanide 
• 6621-59-6 6-bromo-1-hexanenitrile 
• 111-24-0 1,5-dibromo-pentane 
• 628-76-2 1,5-dichloropentane 
• 71933-92-1 1-chloro-5-phenoxypentane 
• 1032300-86-9 ((6-azidohexyl)oxy)benzene 
• 51795-97-2 6-bromohexyloxybenzene 
• 108-95-2 phenol 

Downstream Products

• 16728-68-0 6-phenoxyhexan-1-amine 
• 19790-63-7 6-phenoxy-1-hexanal 
• 19176-65-9 Bis-<6-phenoxy-hexyl>-amin 
• 110010-50-9 [2-(5-Phenoxy-pentyl)-1H-imidazol-4-yl]-methanol 
• 110010-84-9 [2-(5-Phenoxy-pentyl)-1H-imidazol-4-yl]-acetonitrile 

Relevant academic research and scientific papers

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

An efficient transformation of primary halides into nitriles through palladium-catalyzed hydrogen transfer reaction

Two-step one-pot transformation of primary halides into corresponding nitriles is successfully achieved. Nucleophilic substitution of primary halides with sodium azide and subsequent palladium-catalyzed hydrogen transfer proceeds smoothly in the presence of sterically bulky ligand dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (XPhos) in acetone to produce nitriles in satisfactory to good yields. This journal is

An efficient oxidation of primary azides catalyzed by copper iodide: A convenient method for the synthesis of nitriles

A wide range of primary azides have been efficiently oxidized by a catalytic amount of CuI and TBHP into their corresponding nitriles in aqueous solution. A variety of oxidizable functional groups were well tolerated under the reaction conditions, and oxidation of secondary azides furnished their corresponding ketones (see scheme; TBHP=tert-butyl hydroperoxide).