160313-49-5

Basic information

• Product Name: Benzonitrile, 4-bromo-3-(dibromomethyl)-
• CAS NO: 160313-49-5
• Molecular Formula: C8H4Br3N
• Molecular Weight: 353.838
• Mol File: 160313-49-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4-bromo-3-(dibromomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4-bromo-3-(dibromomethyl)-(160313-49-5)
• EPA Substance Registry System: Benzonitrile, 4-bromo-3-(dibromomethyl)-(160313-49-5)

Safety Data

• Hazardous Substances Data: 160313-49-5(Hazardous Substances Data)

Upstream product

• 41963-20-6 4-bromo-3-methylbenzonirtile 

Downstream Products

• 1801711-87-4 1-(hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yl)carboxylic acid 
• 905710-72-7 4-bromo-3-((methoxymethoxy)methyl)benzonitrile 
• 905710-66-9 4-bromo-3-(hydroxymethyl)benzonitrile 
• 160313-56-4 2-<2'-(4''-chlorobutyl)-5'-(tetrahydropyran-2'''-yloxy)methyl>phenyl-1,3-dioxolane 
• 160313-53-1 2-<2'-bromo-5'-(tetrahydropyran-2''-yloxy)methyl>phenyl-1,3-dioxolane 
• 160313-51-9 2-(2'-bromo-5'-t-butyldimethylsiloxymethyl)phenyl-1,3-dioxolane 
• 160313-48-4 2-[(2'-bromo-5'-hydroxymethyl)phenyl]-1,3-dioxolane 
• 89003-95-2 3-formaldehyde-4-bromobenzonitrile 
• 160313-47-3 2-<<2'-bromo-5'-(2''-hydroxyethoxy)carbonyl>phenyl>-1,3-dioxolane 
• 160313-50-8 2-[(2'-bromo-5'-cyano)phenyl]-1,3-dioxolane 

Relevant articles and documents

Fluorescence sensing based on cation-induced conformational switching: Copper-selective modulation of the photoinduced intramolecular charge transfer of a donor-acceptor biphenyl fluorophore

The fluorescence emission energy of donor-acceptor substituted biphenyls is highly sensitive towards conformational changes of the interannular twist angle. By integrating 4-dimethylamino-4′-cyano-biphenyl into the ligand backbone of a thioether-rich metal receptor we designed a fluorescence sensor that exhibits high selectivity towards copper. Upon metal binding the ligand undergoes a significant conformational change, which induces a strong hypsochromic shift of the photoinduced charge-transfer emission. Steady-state absorption and fluorescence spectroscopy revealed a high affinity towards Cu(I) with a well-defined 1:1 metal-ligand complex stoichiometry. The nature of the conformational changes upon Cu(I) coordination were analyzed in detail by 1H NMR and 2D NOESY experiments. The spectroscopic data provide a coherent picture, which is consistent with a Boltzmann ground-state distribution of several rotamers that are locked into a more flattened geometry upon coordination of Cu(I).

1-HYDROXY-1,3-DIHYDROBENZO[c][1,2]OXABOROLES AND THEIR USE AS HERBICIDES

Provided herein are 1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaboroles and their derivatives, and compositions and methods of use thereof as herbicides.

HETEROARYL ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS

Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions that include the compounds described herein, and methods of using such antagonists of PGD2 receptors, alone or in combination with other compounds, for treating respiratory, cardiovascular, and other PGD2-dependent or PGD2-mediated conditions or diseases.