94959-58-7

Upstream product

• 14062-22-7 ethyl 2-(4-(tert-butyl)phenyl)acetate 
• 95-92-1 oxalic acid diethyl ester 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 105-53-3 diethyl malonate 
• 3288-99-1 4-tert-butylbenzyl cyanide 
• 32857-63-9 4-t-butylphenylacetic acid 
• 26537-19-9 methyl 4-tert-butylbenzoate 
• 19692-45-6 4-tert-butylbenzyl chloride 
• 98-73-7 4-(1,1-dimethylethyl)benzoic acid 
• 105-58-8 Diethyl carbonate 

Downstream Products

• 115169-49-8 2-(4-tert-butylphenyl)propane-1,3-diol 
• 1375102-88-7 C₂₇H₃₈FN₃O₄S₂ 
• 1375102-81-0 C₁₈H₂₈O₃ 
• 1375102-83-2 C₁₈H₂₇N₃O₂ 
• 1375102-85-4 C₁₉H₂₇NO₂S 
• 1375102-92-3 C₁₉H₃₀O₅S 
• 1375102-86-5 C₂₇H₃₉N₃O₄S₂ 

Relevant academic research and scientific papers

Structure-activity relationships and molecular modeling of the N-(3-pivaloyloxy-2-benzylpropyl)-N′-[4-(methylsulfonylamino)benzyl] thiourea template for TRPV1 antagonism

The structure-activity relationships of N-(3-acyloxy-2-benzylpropyl)- N′-4-[(methylsulfonylamino)benzyl] thioureas, which represent simplified RTX-based vanilloids, were investigated by varying the distances between the four principal pharmacophores and a

Highly active and selective catalysts for the formation of α-aryl ketones

Bulky, electron-rich phosphine ligands with a biphenyl backbone, when combined with Pd(OAc)2, give highly active catalysts for the α-arylation of ketones. The ligand 2-methyl-2'-dicyclohexylphosphinobiphenyl is particularly effective, and with

N-disubstituted cycloalkylmethyl amines useful as fungicides

Compounds having plant fungicidal properties are of formula: and stereoisomers thereof, wherein R1 and R2, each represent a hydrogen atom, a halogen atom, or an alkyl group containing from 1 to 4 carbon atoms, R3 and Rsub