186465-97-4

Upstream product

• 92-50-2 2-( N-ethylanilino)ethanol 

Downstream Products

• 186465-99-6 4-[(2-trimethylsiloxy-ethyl)ethylamino]trimethylsilylethynylbenzene 
• 1263086-74-3 4-[2-[ethyl(4-iodophenyl)amino]ethoxy]phenyl acetate 
• 1419402-73-5 C₂₃H₂₉NO₃Si 
• 1419402-74-6 C₂₀H₂₁NO₃ 
• 1419402-75-7 C₄₁H₄₄INO₃ 
• 1419402-76-8 C₆₁H₇₄N₂O₃ 
• 1419402-77-9 C₆₁H₆₄N₂O₆ 
• 1254689-34-3 C₅₇H₆₀N₂O₄ 
• 1419402-71-3 4-(2-(ethyl(4-((trimethylsilyl)ethynyl)phenyl)amino)ethoxy)phenol 
• 1419402-72-4 C₁₈H₁₉NO₂ 
• 1419402-78-0 C₅₇H₅₈Cl₁₀N₈O₄P₆ 
• 186466-00-2 4-(N-ethyl-N-(2-hydroxyethyl)amino)-phenylacetylene 
• 1303539-39-0 2-(ethyl(4-((trimethylsilyl)ethynyl)phenyl)amino)ethanol 

Relevant academic research and scientific papers

A novel donor-π-acceptor halochromic 2,6-distyrylnaphthalene chromophore: synthesis, photophysical properties and DFT studies

In this study a new 2,6-distyryl naphthalene [2-((4-((E)-2-(6-((E)-2,4-bis(methylsulfonyl)styryl)naphthalen-2-yl)vinyl)phenyl)(ethyl)amino)ethan-1-ol;ASDSN] was synthesized successfully using Heck chemistry as the main reaction. TheASDSNcompound is a dono

A cheap and efficient method for selective para-iodination of aniline derivatives

A new and cheap protocol for controlled iodination in the para-position of various aniline derivatives is presented. It operates under mild conditions by reacting the aniline derivatives with molecular iodine in a mixture of pyridine/dioxane (1/1 vol) at 0°C.

Poling and crosslinking processes in NLO polymers

A series of photocrosslinkable polymers bearing hyperpolarizable side chain chromophores was synthesized, poled and evaluated on the basis of the thermal stability of Second Harmonic Generation (SHG). Photoinitiation allowed for control of the onset of curing. Crosslinking was monitored by infrared spectroscopy and optimal conversion was achieved by applying a slow temperature ramp during exposure. The ultimate stability of the poled polymers was directly related to the number of crosslinking substituents that were attached to the chromophore pendant group. With two reactive groups per chromophore significant SHG was retained at temperatures above the initial polymer glass transition temperature.

The synthesis, characterization and third-order nonlinear optical character of poly(2,5-dipropargyloxybenzoate) containing a polar aromatic diacetylene

The glass transition temperature of the novel compound, poly(2,5-dipropargyloxybenzoate) containing a polar aromatic diacetylene was 105 °C and differential scanning calorimetry showed two exothermic peaks due to the opening of the hexa-2,4-diynylene-1,6-

Synthesis of hydroxyalkyl-substituted, push-pull chromophores based on diphenylacetylenes and 1,4-bis(phenylethynyl)benzenes

Six new push-pull chromophores based on phenylacetylenes were prepared: two 1,2-diphenylacetylenes and four 1,4-bis(phenylethynyl)benzenes. The donor amino groups have hydroxyethyl substituents, and the acceptor groups are cyano or nitro. More soluble ver

A modular approach to two-photon absorbing organic nanodots: Brilliant dendrimers as an alternative to semiconductor quantum dots?

Nanoscopic fluorescent dendrimers having up to 96 two-photon chromophores and showing very large two-photon absorption cross-sections (up to 56 000 GM) were designed as a complementary "organic" alternative to quantum dots. The Royal Society of Chemistry

Synthesis of new crosslinkable co-polymers containing a push-pull zinc porphyrin for non-linear optical applications

In this paper, the synthesis of a crosslinkable co-polymer containing new push-pull arylethynyl zinc porphyrins is described. The synthesis of porphyrin chromophores, analogous to Therien's porphyrin (J. Am. Chem. Soc. 1996, 118, 1497-1503) functionalized

Ablatively photodecomposable compositions

The present invention provides an ablatively photodecomposable polymer having a photoabsorber bound to the polymer (the "ablatively photodecomposable polymer") which does not phase separate, nor does it crystallize. The ablatively photodecomposable polyme