165190-62-5 Usage
General Description
4-Benzyloxy-2-bromonitrobenzene is a chemical compound with the molecular formula C13H10BrNO3. It consists of a benzene ring with a benzyloxy group and a bromo group attached to it, as well as a nitro group in the para position. 4-Benzyloxy-2-bromonitrobenzene is commonly used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It is important to handle this chemical with care, as it may be harmful if swallowed, inhaled, or comes into contact with the skin. Additionally, it should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials.
Check Digit Verification of cas no
The CAS Registry Mumber 165190-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,1,9 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 165190-62:
(8*1)+(7*6)+(6*5)+(5*1)+(4*9)+(3*0)+(2*6)+(1*2)=135
135 % 10 = 5
So 165190-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H10BrNO3/c14-12-8-11(6-7-13(12)15(16)17)18-9-10-4-2-1-3-5-10/h1-8H,9H2
165190-62-5Relevant articles and documents
AMPHIPATHIC AND OTHER DOUBLE-SIDED ALPHA-HELIX MIMETICS BASED ON A 1,2-DIPHENYLACETYLENE SCAFFOLD
-
, (2014/09/29)
Small-molecule scaffolds based on 1,2-diphenylacetylene that accurately replicate the spatial and angular projections of several side chains on both faces of an α-helix, specifically the i and i+7 side chains on one face, and the i and i+2 side chains on the other. The amphipathic α-helix mimetic can be used to disrupt disease-promoting protein-protein interactions that are mediated by α-helices.
Heterocycle annulation of enolizable vinyl quinone imides. Dihydroquinolines and quinolines from thermal 6π-electrocyclizations and indoles from photochemical cyclizations
Parker, Kathlyn A.,Mindt, Thomas L.
, p. 4265 - 4268 (2007/10/03)
(equation presented) Enolizable vinyl quinone mono-and diimide substrates yield protected 6-hydroxy and 6-amino dihydroquinolines by thermal electrocyclization. Aromatization provides the corresponding quinolines in quantitative yields. The quinone monoimide substrates undergo clean photochemical conversion to 5-hydroxy indoles.
