85216-74-6

Upstream product

• 15949-84-5 11-bromoundecanoyl chloride 
• 75-65-0 tert-butyl alcohol 
• 2834-05-1 11-bromoundecanoic acid 
• 115-11-7 isobutene 
• 407-25-0 trifluoroacetic anhydride 

Downstream Products

• 1026800-59-8 [(S)-5-[(S)-3-tert-Butoxy-2-(11-imidazol-1-yl-undecanoylamino)-propionylamino]-5-(2-cyclohexyl-ethylcarbamoyl)-pentyl]-carbamic acid tert-butyl ester 
• 405157-54-2 4'-(1-methyl-heptyloxy)-3'-nitro-biphenyl-4-carboxylic acid 4'-(10-tert-butoxycarbonyl-decyloxy)-biphenyl-4-yl ester 
• 405157-53-1 4''-[10-(tert-butyloxycarbonyl)decyloxy]phenyl 4-[4'-(2-(R)-octyloxy)-3'-nitrophenyl]benzoate 
• 405157-55-3 4''-[10-(hydroxycarbonyl)decyloxy]phenyl 4-[4'-(2-(R)-octyloxy)-3'-nitrophenyl]benzoate 
• 405157-52-0 tert-butyl 11-(4-hydroxy-phenyloxy)undecanoate 
• 2834-05-1 11-bromoundecanoic acid 

Relevant academic research and scientific papers

Liquid crystalline dendrimers containing photoactive cinnamate units

Cinnamate-containing dendrimers have been prepared by peripheral functionalization of the amine groups of a poly(propyleneimine) dendrimer with 4-methoxycinnamate- or 4-(N,N-dimethylamino)cinnamate-derived units and/or 4-cyanobiphenyl units in different p

Electrochemical Response of the Threading/de-threading Process of Calix[6]arene-based Pseudorotaxanes Anchored on Glassy Carbon Electrodes

The development of functional materials and smart surfaces has received tremendous attention in recent years. The anchoring of molecular machines and the transfer of their properties on to solid substrates may facilitate the design of new smart devices. H

CONTRAST AGENTS ENDOWED WITH HIGH RELAXIVITY

The present invention relates to a novel class of paramagnetic ion-based contrast agents of formula (I), wherein a chelating backbone moiety is highly functionalized by the presence of one or more polyhdroxylated chain, that show a pharmacokinetic profile analogous to that of the commonly used T1-general extravascular agents (NSA) but are further characterized by a higher relaxivity.

Preparation of mesogen-functionalized dendrimers for second-order nonlinear optics

Liquid crystalline dendrimers with peripheral mesogen-containing units have been prepared. Multistep synthesis with several selective reactions was used in the preparation of the mesogen-containing molecules, 4″-[10-(hydroxycarbonyl)decyloxy]phenyl 4-[4′-

Synthesis of ω-(2-oxocyclododecyl)alkanoic acids by alkylation of cyclododecanone with ω-haloalkanoic esters under conditions of phase-transfer catalysis

ω-(2-Oxocyclododecyl)alkanoic acids have been obtained by alkylation of cyclododecanone with alkyl 3-bromopropionate, 5-iodopentanoate, and 11-bromoundecanoate under conditions of phase transfer catalysis. - Key words: cyclododecanone, phase-transfer catalysis, alkylation, alkyl ω-haloalkanoates.