3256-44-8

Upstream product

• 24083-16-7 4-(decyloxy)benzaldehyde 
• 5519-23-3 p-decyloxybenzoic acid 
• 112-29-8 1-bromo dodecane 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 62443-10-1 methyl 4-decyloxybenzoate 

Downstream Products

• 2417-71-2 p-Decyloxybenzylbromid 
• 110482-74-1 1-chloromethyl-4-decyloxybenzene 
• 24083-16-7 4-(decyloxy)benzaldehyde 
• 5593-82-8 N-Phe- 
• 5009-57-4 N--Phe-benzylester 
• 5519-08-4 4-Decyloxy-benzyloxy-carbonyl-azid 
• 163118-06-7 3'-carboethoxy-2-[4-decyloxyphenyl]methoxy-[1,1'-biphenyl]-6-acetic acid, ethyl ester 
• 64518-60-1 p-{[p-(Decyloxy)benzyl]amino}benzoic acid 
• 150547-03-8 4-(4-Decyloxy-benzyloxy)-2-hydroxy-benzaldehyde 

Relevant academic research and scientific papers

Novel hydrophobically modified ethoxylated urethanes end-capped by percec-type alkyl substituted benzyl alcohol dendrons: Synthesis, characterization, and rheological behavior

Novel dendron hydrophobically modified ethoxylated urethanes (DHEUR) with almost the same molecular weights, molecular weight distributions, and identical hydrophilic portion but different terminal hydrophobic group numbers were prepared by using Percec-t

1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: A versatile smectogenic moiety

The merger of ionic liquid and liquid crystal fields, obtained by using the imidazolium ring as a common element, has allowed us to tailor a new set of materials which associate specific functionalities. These functionalities are consequences of the origi

Amphiphilic dendritic dipeptides and their self-assembly into helical pores

An amphiphilic dendritic dipeptide, comprises a dipeptide(s) comprising one or more of a naturally occurring or synthetic amino acids and a dendron. These are suitable for use in various formulations, films, coatings, membranes and sensors, among other ap

Smectic Bimetallomesogens: Synthesis and Mesomorphic Properties in Oxygen-Bridged Dicopper and Divanadyl Complexes

The synthesis and mesomorphic properties of a homologous series of N-(3-hydroxypropyl)-4-alkoxylsalicylaldimine, N-(3-hydroxypropyl)-4-(4′-alkoxybenzoxy)salicylaldimine, and their dicopper(II) and dioxovanadium(VI) complexes are reported. Copper complexes

Substituent Effects on Chemosterilant Activity of 2,4-Di-tert-butyl-6-(4'-substituted benzyl)phenols in the House Fly (Musca domestica L.)

A series of 2,4-di-tert-butyl-6-(4'-X-benzyl)phenols was prepared, analogous to the compound Jurd 2644 (X = OMe) in an attempt to establish a Hammett relationship between the 4'-substituent and the chemosterilant activity of the compounds after oral administration to adult Musca domestica.Fourteen compounds of this type were prepared, 12 of them new.Jurd 2419 (X = H) was found to be as active in our bioassay as Jurd 2644, as were four new compounds .All prevented successful reproduction at 30 mg/kg of diet.There was no correlation between Hammett ? and activity.Active compounds all had small substituents and molecular weights below 350.The activity seemed to be determined by the bulk of X rather than by its electronic properties. - Keywords: Reproduction; delayed toxicity; Jurd 2644

BIARYL PHOSPHOLIPASE A2 INHIBITORS

Certain novel biaryl compounds are effective phospholipase A2 (PLA2) inhibitors.

Sebosuppressive preparations containing alkoxyaryl alkanols

Substituted benzyl alcohols and substituted phenyl ethanols which are novel and the use of these and related compounds known per se, as sebosuppressives.

Antilipidemic para-[aryl(alkyl or alkenyl)amino]-benzoic acid derivatives

Novel para-[aryl(alkyl or alkenyl)amino]benzoic acids, esters, pharmaceutically acceptable salts and pharmaceutical compositions thereof and a method of lowering serum lipid levels in mammals therewith.