scholarly journals 2-(Fluoromethyl)-4,7-dimethoxy-1-methyl-1H-benzimidazole

Molbank ◽  
10.3390/m1129 ◽  
2020 ◽  
Vol 2020 (2) ◽  
pp. M1129
Author(s):  
Patrick Kielty ◽  
Pau Farràs ◽  
Dennis A. Smith ◽  
Fawaz Aldabbagh

Selectfluor (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)) substitutes the TEMPO free radical with fluorine on 4,7-dimethoxy-1-methyl-2-{[(2,2,6,6-tetramethylpiperidin-1-yl)oxy]methyl}-1H-benzimidazole to give the title compound in a 77% yield. A mechanism is proposed for the formation of this novel methylene fluoride.

2013 ◽  
Vol 69 (12) ◽  
pp. o1792-o1793
Author(s):  
Praveen Pitliya ◽  
Ray J. Butcher ◽  
A. Karim ◽  
Paul F. Hudrlik ◽  
Anne M. Hudrlik ◽  
...  

The title compound, C22H30BrNO, is an alkoxyamine compound, an effective initiator in nitroxide-mediated free radical polymerization. It was prepared as a mixture of two diasteromers; the crystal for the X-ray analysis showed one of these as a pair ofR,SandS,Renantiomers. Thetert-butyl and isopropyl groups are in an almostanticonformation in the crystal [C—N—C—C torsion angle = −168.8 (1)°], and the methyl group of the ethoxy group is in an approximateantirelationship to thetert-butyl group. The dihedral angle between the phenyl and benzene rings is 33.12 (7)°. The Br atom is disordered over two positions, with occupancies of 0.9139 (16) and 0.0861 (16). In the crystal, weak C—H...Br contacts link the molecules into chains along [-110].


1968 ◽  
Vol 21 (6) ◽  
pp. 1571 ◽  
Author(s):  
W Davies ◽  
BC Ennis ◽  
QN Porter

It is shown that heat in the absence of a solvent converts the title compound into benzo[k,l]thioxanthen 7,7-dioxide, 7-thiabenzo[c]fluorene, and o-(1-naphthyl)-benzenesulphonic acid. From these results and a consideration of the related pyrolyses of the 3,10- and 1,8-dimethyl derivatives of the title compound, a free-radical rearrangement mechanism is proposed to explain the observations.


2006 ◽  
Vol 62 (7) ◽  
pp. o2734-o2735 ◽  
Author(s):  
Rodolfo Moreno-Fuquen ◽  
Hoover Valencia ◽  
Zulay Diney Pardo ◽  
Richard D'Vries ◽  
Alan R. Kennedy

The title compound, C10H6N2O4, belongs to a series of N-arylmaleimides, which can be used as photoinitiators for free-radical polymerization. The dihedral angles between the planes of the benzene and imide rings are 56.2 (1) and 52.9 (1)° in the two independent molecules in the asymmetric unit.


2017 ◽  
Vol 72 (2) ◽  
pp. 89-94 ◽  
Author(s):  
Alexandru T. Balaban ◽  
Titus Constantinescu ◽  
Miron Teodor Caproiu ◽  
Michel Giorgi ◽  
Teodor Silviu Balaban

AbstractThe title compound is formed by a non-trivial reaction involving two molecules of the stable free radical 2,2-diphenyl-1-picryl-hydrazyl and one molecule of N-methoxy-picramide. We could now perform an X-ray diffraction experiment on a single crystal and can fully confirm the betaine structure which has a central quinonoid ring with alternating long and short bonds.


Author(s):  
O. M. Faroon ◽  
R. W. Henry ◽  
M. G. Soni ◽  
H. M. Mehendale

Previous work has shown that mirex undergoes photolytic dechlorination to chlordecone (CD) (KeponeR) in the environment. Much work has shown that prior exposure to nontoxic levels of CD causes potentiation of hepatotoxicity and lethality of CCl4, BrCCl3 and other halomethane compounds. Potentiation of bromotrichloromethane hepatotoxicity has been associated with compounds that stimulate the activity of hepatic mixed-function oxidase (MFO). An increase in the metabolism of halomethane by the MFO to a free radical initiates peroxidative decomposition of membranal lipids ending in massive cellular injury. However, not all MFO inducers potentiate BrCCl3 hepatotoxicity. Potentiation by much larger doses of phenobarbital is minimal and th at by a more potent inducer of MFO, mirex, is negligible at low doses. We suggest that the CD and bromotrichloromethane interaction results in a depletion of cellular energy and thereby reducing the cellular ability to undergo mitosis.


Author(s):  
Fengqian Zhao ◽  
Xiao-Feng Wu

A transition-metal-free radical carbonylation of activated alkylamines with thiophenols has been successfully developed. Various thioesters were selectively produced with moderate to good yields.


2004 ◽  
Vol 171 (4S) ◽  
pp. 295-295
Author(s):  
Fernando C. Delvecchio ◽  
Ricardo M. Brizuela ◽  
Karen J. Byer ◽  
W. Patrick Springhart ◽  
Saeed R. Khan ◽  
...  

2005 ◽  
Vol 2 (2) ◽  
pp. 107-109
Author(s):  
A. Mishra ◽  
M.F. Huda ◽  
V.P. Singh ◽  
S. Mohanty ◽  
A. Sodhi

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