45739-16-0

Upstream product

• 608-30-0 2,6-dibromoaniline 

Downstream Products

• 67385-03-9 C₁₄H₁₂Br₂NO 
• 67384-83-2 C₇H₆Br₂NO 
• 35128-56-4 4-bromo-7-nitro-2,1,3-benzoxadiazole 
• 35036-93-2 4-bromobenzo[c][1,2,5] oxadiazole 
• 916853-02-6 μ2-(η2-N,O-2,6-dibromonitrosobenzene)bis[μ-chlorotricarbonylrhenium(I)] 
• 916853-03-7 μ2-(η2-N,O-2,6-dibromonitrosobenzene)bis[μ-bromotricarbonylrhenium(I)] 
• 501665-35-6 3-bromo-2-(tert-butyl-NNO-azoxy)aniline 
• 514206-60-1 2,6-dibromo(tert-butyl-NNO-azoxy)benzene 
• 13402-32-9 1,3-dibromo-2-nitrobenzene 

Relevant academic research and scientific papers

Diastereoselective intermolecular ene reactions: Synthesis of 4,5,6,7-tetrahydro-1H-benzo[d]imidazoles

The Diels-Alder cycloadducts of 4-vinylimidazoles and N-phenylmaleimide are shown to undergo facile intermolecular ene reactions. Overall the reaction of three simple molecules (a diene, a dienophile and an enophile) in a two-step process gives 4,5,6,7-te

NOVEL BRIDGED BICYCLOALKYL-SUBSTITUTED AMINOTHIZOLES AND THEIR METHODS OF USE

The present invention includes novel bridged bicycloalkyl-substituted aminothiazole compounds useful in preventing or treating cancer in a subject in need thereof. The present invention also includes methods of preventing or treating cancer in a subject i

Small Molecule Agonists and Antagonists of NR2F6 Activity in Humans

The present technology is directed to modulators of nuclear receptor activity, specifically to the modulation of NR2F6 activity and NR2F6 utilizing compounds, and the immune modulation and modulation of cancer stem cell activity through administration of

Syntheses of shuttlecock- and bowl-equipped phenylazopyridines and photomodulation of their coordination ability to Zn-porphyrin

Shuttlecock- and bowl-equipped 4-(phenylazo)pyridine derivatives, which bear substituents that allow the pyridine moiety to protrude in the trans form but hinder it in the cis form, have been designed and synthesized. These molecules show cis/trans photoisomerization despite the presence of bulky substituents. 1H NMR titration with Zn-porphyrin showed that the trans isomers coordinate to Zn-porphyrin much stronger than the cis isomers.

METHOD AND MEANS RELATING TO MULTIPLE HERBICIDE RESISTANCE IN PLANTS

Methods for overcoming multiple herbicide resistance (MHR) in plants using inhibitors of GST suppression of Formula (I), novel chemical inhibitors of Formula (Ia), compositions comprising compounds of Formula (I), and uses and methods relating thereto.

Nucleophilic substitution in benzo-1,2,3,4-tetrazine 1,3-dioxides

Nucleophilic substitution in nitro- and bromobenzo-1,2,3,4-tetrazine 1,3-dioxides (BTDOs) was studied. In most cases, the bromo and nitro groups are replaced by methylamino, dimethylamino, azido, and methoxy groups without opening of the tetrazine ring. I

Pyrrolidine modulators of chemokine receptor activity

The present invention is directed to pyrrolidine compounds of the formula 1: (wherein R1, R2, R3, R4, R5, R6and n are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-5 and/or CCR-3.

Designing banana-shaped liquid crystals without Schiff's base units: m- Terphenyls, 2,6-diphenylpyridines and V-shaped tolane derivatives

This paper reports attempts to obtain (anti)ferroelectric switchable achiral banana-shaped molecules without Schiff's base units. For this purpose we have synthesized novel V-shaped molecules consisting of rigid angular central units [1,3-disubstituted be

PRESSURE EFFECT ON DIMERIZATION EQUILIBRIA OF A SERIES OF SUBSTITUTED NITROSOBENZENES IN SOLUTION.

The effect of pressure was studied on the dimerization reactions of six di- and tri-substituted nitrosobenzenes in carbon tetrachloride at 25 degree C. The obtained configurational volume changes for the prototype one bond formation reactions are in the range of minus 17 to minus 21 cm**3 mol** minus **1 at 6. 13 MPa. The volume changes were interpreted in terms of the perturbation theory of liquid; they were dominated by the volume change in the reference system composed of hard spheres. Small differences between the observed and theoretical reference volume changes were ascribed to the perturbation due to electrostatic interactions between the solute and solvent; the perturbation volume changes were estimated by the Kirkwood theory of dipolar solvation.