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Trans-α-phenyl-α-[6-phenyl-6-(2-pyridyl)-2-fulvenyl]-2-pyridinemethanol is a complex organic compound characterized by its unique molecular structure. It features a phenyl group (C6H5) attached to a pyridine ring, which in turn is connected to a fulvene moiety, a type of aromatic compound with a five-membered ring containing four carbon atoms and one double-bonded oxygen atom. The fulvene ring in trans-α-phenyl-α-[6-phenyl-6-(2-pyridyl)-2-fulvenyl]-2-pyridinemethanol is further adorned with a phenyl group and a pyridyl group, enhancing its aromatic character. This molecule is known for its potential applications in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other specialty chemicals, due to its intricate structure and the possibility of forming various interactions with other molecules.

6602-58-0

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6602-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6602-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6602-58:
(6*6)+(5*6)+(4*0)+(3*2)+(2*5)+(1*8)=90
90 % 10 = 0
So 6602-58-0 is a valid CAS Registry Number.

6602-58-0Downstream Products

6602-58-0Relevant academic research and scientific papers

Stereoselective synthesis of the rat selective toxicant norbormide

Jay-Smith, Morgan,Murphy, Elaine C.,Shapiro, Lee,Eason, Charles T.,Brimble, Margaret A.,Rennison, David

, p. 5331 - 5342 (2016/08/04)

Norbormide [5-(α-hydroxy-α-2-pyridylbenzyl)-7-(α-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide] (NRB, 1), an existing but infrequently used rodenticide, is known to be uniquely toxic to rats but relatively harmless to other rodents/mammals. However, as an acute vasoactive, NRB has a rapid onset of action which makes it relatively unpalatable to rats, often leading to sub-lethal uptake/accompanying bait shyness. It is recognized that the pharmacological profile of NRB is highly sensitive to its stereoisomeric composition, yet no comprehensive endeavor has been made to impart any stereochemical control in its manufacture. The effect of temperature/concentration/reaction solvent/Lewis acid on the Diels–Alder synthesis of NRB is investigated. An attempted stereoselective synthesis of key NRB precursor 2-fulvenylmethanol 4 is also described. Palatability/efficacy data in rats is reported for novel NRB batches 1a–1e. Disappointingly, given the level of stereocontrol now available in the synthesis of NRB as a result of this research, no clear relationship between stereoisomeric composition and palatability was observed.

RODENTICIDAL NORBORMIDE ANALOGUES

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Page/Page column 83, (2013/09/26)

The present invention relates to norbormide analogues having rodenticidal activity; rodenticidal compositions comprising the analogues; uses of the analogues as rodenticides; uses of the analogues in the manufacture of rodenticidal compositions; and methods for controlling rodents using the compositions.

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