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Cis-α-phenyl-α-[6-phenyl-6-(2-pyridyl)-2-fulvenyl]-2-pyridinemethanol is a complex organic compound with a molecular formula of C27H21N2O. It is characterized by a unique structure that includes a phenyl group, a pyridine ring, and a fulvene moiety. The fulvene part of the molecule features a six-membered ring with alternating double bonds, which is fused to a phenyl ring and a pyridine ring. The presence of these functional groups gives the compound potential applications in various fields, such as pharmaceuticals, materials science, and organic chemistry research. Due to its specific geometric arrangement, the "cis" configuration indicates that the phenyl and pyridine groups are on the same side of the double bond in the fulvene ring. cis-α-phenyl-α-[6-phenyl-6-(2-pyridyl)-2-fulvenyl]-2-pyridinemethanol's properties and reactivity can be influenced by its stereochemistry, making it an interesting subject for further study and potential applications.

6586-38-5

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6586-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6586-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6586-38:
(6*6)+(5*5)+(4*8)+(3*6)+(2*3)+(1*8)=125
125 % 10 = 5
So 6586-38-5 is a valid CAS Registry Number.

6586-38-5Downstream Products

6586-38-5Relevant 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)

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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