99858-53-4

Upstream product

• 821-09-0 n-Pent-4-enyl alcohol 
• 1119-51-3 bromopentene 
• 100-02-7 4-nitro-phenol 
• 19300-54-0 toluene-4-sulfonic acid pent-4-enyl ester 
• 123-30-8 4-amino-phenol 
• 1124-31-8 potassium 4-nitrophenolate 
• 99855-58-0 1-nitro-4-(pent-4-en-1-yloxy)benzene 

Downstream Products

• 1582787-98-1 4,6-di(2-phenylpropan-2-yl)-2-{[4-(pent-4-enyloxy)phenylimino]methyl}phenol 
• 1421313-45-2 bis[2-{[4-(pent-4-enyloxy)phenylimino]methyl}-4,6-di(2-phenylpropan-2-yl)phenoxy]titanium(IV) dichloride 
• 1582787-99-2 2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(2-phenylpropan-2-yl)-4-chlorophenol 
• 1582788-12-2 bis[2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(2-phenylpropan-2-yl)-4-chlorophenoxy]titanium(IV) dichloride 
• 1582788-00-8 4-bromo-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(2-phenylpropan-2-yl)phenol 
• 1582788-13-3 bis[4-bromo-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(2-phenylpropan-2-yl)phenoxy]titanium(IV) dichloride 
• 1582788-01-9 2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenol 
• 1582788-14-4 bis[2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenoxy]titanium(IV) dichloride 
• 1582788-02-0 4-methyl-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenol 
• 1582788-15-5 bis[4-methyl-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenoxy]titanium(IV) dichloride 
• 1582788-03-1 4-tert-butyl-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenol 
• 1582788-16-6 bis[4-tert-butyl-2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)phenoxy]titanium(IV) dichloride 
• 1582788-04-2 2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)-4-chlorophenol 
• 1582788-17-7 bis[2-{[4-(pent-4-enyloxy)phenylimino]methyl}-6-(1-phenylethyl)-4-chlorophenoxy]titanium(IV) dichloride 

Relevant academic research and scientific papers

Decoquinate derivatives: A new class of potent antischistosomal agents against Schistosoma japonicum

Decoquinate (1), an old and inexpensive coccidiostat, exhibited potent antimalarial activity, however, its antischistosomal activity against Schistosoma japonicum has not yet been evaluated. Based on decoquinate, a series of decoquinate derivatives was designed, synthesized, evaluated as a new class of antischistosomal agents against S. japonicum adult worms in vitro. Among them, compound 15 killed 100% of adult S. japonicum in 72?h at the concentration of 10?μmol/L in vitro, exhibited stronger worm-killing activity than PZQ in vitro and could serve as a promising lead compound to develop new antischistosomal agents.

Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XVI. Synthesis of (N-aryl)salicylaldimines containing pent-4-enyloxy group and their complexes with titanium(IV) dichloride

Reactions of p-(pent-4-enyloxy)aniline with salicylaldehyde containing versatile substituents in the positions 3 and 5 in an open system without solvent at 130°C afforded a series of (N-aryl)salicylaldimines, which with TiCl2(OPr-i)2 formed complexes of titanium(IV) dichloride L2TiCl2.

Soluble polymer synthesis: An improved traceless linker methodology for aliphatic C-H bond formation

A traceless linker was developed on a soluble polymer support. The methodology allows for the facile attachment of molecules possessing an alkyl halide appendage. The coupled molecule can be further functionalized before subsequent cleavage via a two-step oxidation-reduction sequence. This sequence allows for the synthesis of molecules containing no trace of the linker and the formation of a new C-H bond.