40141-11-5

Upstream product

• 5736-85-6 4-propoxybenzaldehyde 
• 90925-43-2 4-n-propyloxybenzyl alcohol 
• 622-85-5 propoxybenzene 

Downstream Products

• 100966-20-9 diethyl-(4-propoxy-benzyl)-amine 
• 21244-33-7 1-(4-propoxyphenyl)methanamine 
• 169610-45-1 ethyl N-(4-propoxyphenylmethyl)piperidin-4-yl carboxylate 
• 101715-05-3 (4-propoxy-benzyl)-carbamic acid methyl ester 
• 515871-66-6 ((4S,5S)-5-{[Bis-(4-propoxy-benzyl)-amino]-methyl}-2,2-dipropyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-propoxy-benzyl)-amine 
• 515871-39-3 ((4S,5S)-5-{[Bis-(4-propoxy-benzyl)-amino]-methyl}-2-tert-butyl-2-methyl-[1,3]dioxolan-4-ylmethyl)-bis-(4-propoxy-benzyl)-amine 
• 50690-52-3 (4-propoxy-phenyl)-acetonitrile 
• 5736-85-6 4-propoxybenzaldehyde 

Relevant academic research and scientific papers

Design, synthesis and antiproliferative activity of tripentones: A new series of antitubulin agents

Structure-activity relationship studies of a new series of tripentones (thieno[2,3-b]pyrrolizin-8-ones), led us to prepare several derivatives with antiproliferative activities. The most promising 3-(3-hydroxy-4-methoxyphenyl)thieno[2,3-b]pyrrolizin-8-one 20 (leukemia L1210, IC50 = 15 nM) was shown to be a potent inhibitor of tubulin polymerization.

Insecticidal N-(substituted arylmethyl)-4-[bis(substituted phenyl or pyridyl)methyl]piperidines

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts thereof, are disclosed as effective insecticides: whereinU is —(CH2)n—;Q is hydroxy; andR is: and whereinV, W, Y, and Z are each hydrogen;X is a five- or six-membered heterocycle; optionally substituted with bromine, chlorine, fluorine, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkoxyalkyl, haloalkoxyalkyl, or aminocarbonyl; and the heterocycle is optionally connected to the phenyl ring through a —O—, —S—, —(CH2)p, —C(O)—, or —O—(CR3R4)q linkage;R1 and R2 are independently selected from phenyl or pyridyl substituted with pentahalothio, haloalkylthio, haloalkylsulfinyl, or haloalkylsulfonyl; phenyl substituted with —OC(M)2O—, where M is bromine, chorine or fluorine, to provide a dihalobenzodioxolyl fused ring; or pyridyl substituted with —OC(M)2O— to provide a dihalodioxolenopyridyl fused ring;R3 and R4 are independently selected from hydrogen and methyl;n and p are independently 1, 2, or 3; andq is 1 or 2; with the proviso that at least one of R1 and R2 is substituted in the para position of the phenyl ring or the 5-position of the 2-pyridyl ring; each alkyl portion of said optional substituent on X wherein the optional substituent is alkyl, haloalkyl, alkoxyl, haloalkoxyl, alkoxyalkyl, or haloalkoxyalkyl contains from 1 to 4 carbon atoms; each heterocycle contains from 1 to 4 nitrogen atoms, 1 or 2 oxygen or sulfur atoms, or 1 or 2 nitrogen atoms and an oxygen or sulfur atom; and the corresponding N-oxides and agriculturally acceptable salts.

Insecticidal compositions containing n-(substituted phenylmethyl)-4-[bis(substituted phenyl)methyl]piperidines

Compositions containing compounds of the following structure, some of which are novel, and the corresponding N-oxides and agriculturally acceptable salts, are disclosed as effective insecticides: in which U is -(CH2)n-; Q is hydroxy; R is in which V, W, a

Insecticidal N-(substituted arylmethyl)-4-?bis(substituted aryl)hydroxymethyl!piperidinium salts

Compounds of the following structure are disclosed as effective insecticides: STR1 in which Q is hydroxy; U is --(CH2)n --, where n is 1; R is STR2 in which V, W, Y, and Z are each hydrogen; X is alkoxy, cycloalkylalkoxy, alkoxycarbo

Insecticidal N-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts, are disclosed as effective insecticides: STR1 in which U is selected from --(CH2)n -- and ethylidene; Q is selected from hydrogen, hydroxy, sulfhydryl, and fluorine; R is STR2 in which V is selected from hydrogen, halogen, alkyl, haloalkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsilyloxy, dialkylamino, cyano, nitro, hydroxy, and phenyl; Y and Z are independently selected from hydrogen and alkoxy; W and X taken together is --OCH2 CH2 O--, --CH2 C(CH3)2 O--, --OC(CH3)2 O--, or --N=C(C2 H5)O--; R1 and R2 are independently selected from phenyl substituted with halogen, alkyl, haloalkyl, haloalkoxy, alkoxyalkyl, hydroxy, arylthio, alkoxy, dialkylamino, dialkylaminosulfonyl, hydroxyalkylaminocarbonyl, alkylsulfonyloxy, and haloalkylsulfonyloxy; and n is 1, 2, or 3.

Insecticidal n-(substituted arylmethyl)-4-[bis(substituted phenyl) methyl]pi

Compounds of the following structure, the corresponding N-oxides and agriculturally acceptable salts, are disclosed as effective insecticides: STR1 in which U is selected from STR2 Q is selected from hydrogen, hydroxy, sulfhydryl, and fluorine; R is selected from a heterocycle having 5 or 6 ring atoms, optionally fused to a benzene ring, and STR3 wherein V, W, X, Y, Z are as defined in the specification.