84349-14-4

Upstream product

• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 3673-06-1 N,N'-dicyclohexylethylenediimine 
• 108-91-8 cyclohexylamine 

Downstream Products

• 84348-93-6 N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-N-cyclohexylacetamide 

Relevant academic research and scientific papers

A simple synthesis of 3,4-dihydrobenzo[f]quinoxalin-6(2H)-one derivatives substituted in the ring B

[Figure not available: see fulltext.] We followed a simple, inexpensive, and efficient route to synthesize a series of 3,4-dihydrobenzo[f]quinoxalin-6(2H)-one derivatives substituted in the ring B, with the expectation that this scaffold might exhibit antineoplastic activity. 5-Chlorobenzo[f]quinoxalin-6-ylacetate and 4-benzylbenzo[f]quinoxalin-6(4H)-one were obtained for the first time.

Composition for Distructing Microalgae

The present invention relates to a composition for destroying microalgae, more specifically, to a composition for destroying microalgae containing naphthoquinone compounds having a specific exchange group. The composition for destroying microalgae, according to the present invention, can prevent green tide and red tide by being processed in areas such as cultivation facilities for microalgae, areas in which the green tide or the red tide occur, or areas expected to occur the green tide or the red tide.

Identification of unusual C-Cl...π contacts in 2-(alkylamino)-3-chloro-1,4-naphthoquinones: Effect of N-substituents on crystal packing, fluorescence, redox and anti-microbial properties

The chemo-selective reaction of 2,3-dichloro-1,4-naphthoquinone with different primary amines affords access to a series of derivatives, such as 2-(alkylamino)-3-chloro-1,4-naphthoquinone (1-6) and 2-(benzylamino)-1,4-naphthoquinone (7), in good yields. All the compounds 1-7 were characterized thoroughly by microanalysis, standard spectroscopy and thermogravimetric methods. The supramolecular structures of 1-4 and 7 were studied by means of single-crystal X-ray diffraction to gauge the influence of substituents that are present on the amine functionality on the association of molecules in the solid state. The study showed that the introduction of various amine N-substituents induces conformational changes that apparently modify the nature and number of donor-acceptor sites for noncovalent interactions, leading to diverse crystal packing patterns. Interestingly, the introduction of 2-(benzylamino)- and 2-(2-pyridylmethylamino)- substituents in 2 and 4 successfully switched on the C-Cl...π synthon, which is scarcely seen in the crystal packing of organic molecules. Compounds 1, 2, 4 and 5 fluoresced in the range of 350-620 nm with concomitant Stokes shifts of 81, 131, 141 and 131 nm, respectively, and their cyclic voltammograms evidenced two quasi-reversible single-electron waves. All the compounds (except 5) exhibited their first endothermic peak on the DTA curves without any mass loss due to the phase change, attributable to the melting points of the respective compounds. Remarkably, compound 5 exhibited an enhanced antibacterial activity against S. aureus and proved to be a more potent antibacterial agent than the well-known drug "ciprofloxacin".

NAPHTHAQUINONE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

Provided herein are compounds of (I), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, and prodrugs thereof. Also provided are pharmaceutical compositions and methods involving the inventive compounds for the treatment of proliferative diseases (e.g., cancer (e.g., leukemia, breast cancer, melanoma, metastatic cancer) and diseases associated with inappropriate SET8 activity. Also provided are methods for inhibiting SET8 and methods for labelling SET8.

A new synthesis of quinoxaline, imidazolidine, indole and carbazole derivatives

Reactions of bis-benzalethylenediamine (1), N,N'-bis(aryl)- and N,N'-bis(cyclohexyl)ethane-1,2-diylidenediamines as well as N,N'-bis(aryl)benzene-1,4-diyldimethylidenediamines 2 with benzo- and naphthoquinones as well as α,β-unsaturated ketones such as 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ); 2,3,5,6-tetrachloro-1,4-benzoquinone (CHl-p); 3,4,5,6-tetrachloro-1,2-benzoquinone (CHl-o); 2,3-dichloro-1,4-naphthoquinone (DCNQ); 2,3-dicyano- l,4-naphthoquinone (DCNQ) and dicyanomethyleneindane-1,3-dione (CNIND) afforded quinoxaline, pyrazinoquinoxaline, imidazolidine, indole and carbazole derivatives as well as arylaminobenzo-, and napthoquinones.