77670-29-2

Upstream product

• 75-52-5 nitromethane 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 536-74-3 phenylacetylene 
• 22252-15-9 trans-4-methoxychalcone 
• 123-11-5 4-methoxy-benzaldehyde 
• 70-11-1 α-bromoacetophenone 
• 98-86-2 acetophenone 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 120-46-7 1,3-diphenylpropanedione 
• 123-08-0 4-hydroxy-benzaldehyde 
• 24083-19-0 4-n-dodecyloxybenzaldehyde 

Downstream Products

• 111034-26-5 3-(4-methoxyphenyl)-5-phenyl-3,4-dihydro-2H-pyrrole 
• 850006-86-9 C₃₄H₂₅Br₂N₃O₂ 
• 861033-75-2 4-(4-methoxyphenyl)-2-phenyl-1H-pyrrole 
• 55164-80-2 3-(4-methoxy-phenyl)quinolin-2(1H)-one 
• 85658-00-0 4-(4-methoxyphenyl)-2-phenylfuran 
• 861033-84-3 3-(4-methoxyphenyl)-2-nitroso-5-phenyl-1H-pyrrole 

Relevant academic research and scientific papers

Aza-BODIPY molecular assembly at the liquid-solid interface driven by Br?F[sbnd]BF interactions

In this work, two aza-BODIPY derivatives, 3,5-diphenyl-1,7-di(p-dodecyloxyphenyl)-aza-BODIPY (CJF) and 3,5-di(p-bromophenyl-1,7-di(p-dodecyloxyphenyl)-aza-BODIPY (2Br-CJF) acted as model molecules to form the self-assembly monolayers on the solid-liquid i

Exploring the copper binding ability of Mets7 hCtr-1 protein domain and His7 derivative: An insight in Michael addition catalysis

Mets7 is a methionine-rich motif present in hCtr-1 transporter that is involved in copper cellular trafficking. Its ability to bind Cu(I) was recently exploited to develop metallopeptide catalysts for Henry condensation. Here, the catalytic activity of Me

In vitro photodynamic treatment of cancer cells induced by aza-BODIPYs

Two aza-BODIPY photosensitizers (PSs, compounds 7 and 8), featuring an iodine atom on each pyrrolic unit of their structure, were synthesized in fairly good yields starting from commercial products and tested in vitro on two human cancer cell lines (HCT11

LANTHANIDE COMPLEXES BASED ON TRIETHYLENETETRAMINE-N,N,N',N'',N''',N'''-HEXAACETIC ACID DERIVATIVES

The present invention relates to a complex comprising at least one lanthanide (Ln) and at least one compound (C) comprising a unit of formula (I) below: said unit of formula (I) being covalently connected to at least one antenna which absorbs at a wavelength ranging from 500 nm to 900 nm.

LANTHANIDE COMPLEXES COMPRISING DENDRIMERS

The present invention relates to a complex comprising at least one dendrimer and at least one lanthanide, wherein the dendrimer comprises a unit of formula (I) below: in which: C1 is a valence group 4 of formula >N—CH2—CH2—N1, A2 and A3 are groups of formula —(CH2)2—C(O)—NH—(CH2)2—; the unit of formula (I) being connected covalently to at least one antenna which absorbs at a wavelength ranging from 500 nm to 900 nm.

Sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes: one-step synthesis of 4-nitro-1,3-diarylbutan-1-ones

Abstract : The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild, transition-metal-free condition. This one-step method involving sequential carbon-carbon bond formation and cleavage provides a good alternative to the synthesis of various γ-nitro ketones. Graphical abstract: The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild and transition-metal-free condition. [Figure not available: see fulltext.].

Enantioselective addition of aryl ketones and acetone to nitroalkenes organocatalyzed by carbamate-monoprotected cyclohexa-1,2-diamines

Enantiomerically pure carbamate-monoprotected trans-cyclohexane-1,2-diamines are used as chiral organocatalysts for the addition of aryl ketones and acetone to nitroalkenes to give enantioenriched β-substituted γ-nitroketones. The reaction was performed i

Gold(I) complexes of brominated azadipyrromethene ligands

Azadipyrromethenes are luminescent, red-light absorbing dyes that readily bind BF2+ and metals. Their framework allows for structural modification at the phenyl arms and the two pyrrolic carbon positions. Here we report five new gold

Synthesis, optical properties and ultrafast dynamics of aza-boron-dipyrromethene compounds containing methoxy and hydroxy groups and two-photon absorption cross-section

In this work, aza-boron-dipyrromethene (aza-BODIPY) compounds containing methoxy and hydroxy groups were synthesized. The effects of substitution and intramolecular charge transfer on linear and nonlinear optical absorptions (especially two photon absorpt

Efficient microwave activation of hydrotalcite clays in Michael addition under solvent-free conditions

Microwave irradiation has been successfully utilized for the first time for the activation of unmodified hydrotalcites (HTs, a basic anionic clay), in the Michael addition reaction between enones and active methylenic compounds under solventless condition