169784-42-3

Upstream product

• 66750-10-5 13-phenyl-1,4,7,10-tetraoxa-13-aza-cyclopentadecane 

Downstream Products

• 284687-71-4 phenyl-bis-[4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-methanol 
• 135366-31-3 4-(4,7,10,13-tetraoxa-1-azacyclopentadecyl)benzoic acid 
• 284687-72-5 (4-dimethylamino-phenyl)-phenyl-[4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-methanol 
• 1160928-61-9 13-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,4,7,10-tetraoxa-13-azacyclopentadecane 
• 1265817-34-2 5-(4-(1,4,7,10-tetraoxa-13-azacyclopentadecan-13-yl)phenyl)thiophene-2-carbaldehyde 
• 284687-73-6 tris-[4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-phenyl]-methanol 

Relevant academic research and scientific papers

Elctrophilic bromination of alkenes, alkynes, and aromatic amines with potassium bromide/orthoperiodic acid under mild conditions

Bromination of alkenes, alkynes, and aromatic amines has efficiently been carried out at room temperature in short reaction times using potassium bromide/orthoperiodic acid in dichloromethane-water (1:1) to prepare the corresponding bromo compounds with excellent yields.

A Green protocol for the bromination and iodination of the aromatic compounds using H5IO6/NaBr and H5IO 6/NaI in the water

Bromination and iodination of the aromatic compounds have efficiently been carried out at room temperature and 70 °C, respectively, in short reaction times using orthoperiodic acid/sodium bromide (1:2) and orthoperiodic acid/sodium iodide (1:2) in water to prepare the corresponding halo compounds with excellent yields.

A new recognition concept using dye sensitized solar cell configuration

A bifunctional compound 1 was designed and synthesized, in which the donor-π-conjugated-acceptor-cyanoacrylic acid configuration is suited for DSSC, while the tetraoxa-azacrown (donor) part also acts as the recognition unit for e.g. Ca2+ and th

Electrophilic bromination of alkenes, alkynes, and aromatic amines with iodic acid/potassium bromide under mild conditions

Bromination of alkenes, alkynes, and aromatic amines has efficiently been carried out at room temperature in short reaction times using HIO 3/KBr in CH2Cl2/H2O (1:1) to prepare corresponding brominated compounds in excellent yields.

Methods for preparing metal ion photocages: Application to the synthesis of crowncast

Three different synthetic strategies were utilized in the construction of a novel class of macrocyclic containing o-nitrobenzhydrol group II cation cages. The synthetic methodology presented herein is unparalleled in scope toward the preparation of caged

{[K.18-Crown-6]Br3}n: a unique tribromide-type and columnar nanotube-like structure for the oxidative coupling of thiols and bromination of some aromatic compounds

Reaction of 18-crown-6 with KBr and then with bromine (Br2) afforded a unique tribromide salt with a nanotube-like structure ({[K.18-crown-6]Br3}n). Oxidative coupling of thiols and bromination of some aromatic compounds is the first report on the chemistry of this reagent.

Metal-ion complexation and photochromism of triphenylmethane dye derivatives incorporating monoaza-15-crown-5 moieties

Three types of triphenylmethane leuconitrile derivatives incorporating one, two, and three monoaza-15-crown-5 moieties have been designed to attain photocontrol of metal-ion complexation primarily by intramolecular electrostatic repulsion. Photochromism o