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2-Pyridinecarbonitrile, 6-phenoxy-, also known as 6-phenoxynicotinonitrile, is an organic compound with the chemical formula C12H8N2O. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 2-Pyridinecarbonitrile, 6-phenoxy- is characterized by the presence of a pyridine ring with a nitrile group at the 2-position and a phenoxy group at the 6-position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of insecticides and herbicides. Due to its reactivity and potential applications, 2-Pyridinecarbonitrile, 6-phenoxy- is a compound of interest in the fields of organic chemistry and chemical engineering.

501378-40-1

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501378-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501378-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,3,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 501378-40:
(8*5)+(7*0)+(6*1)+(5*3)+(4*7)+(3*8)+(2*4)+(1*0)=121
121 % 10 = 1
So 501378-40-1 is a valid CAS Registry Number.

501378-40-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-phenoxypicolinonitrile

1.2 Other means of identification

Product number -
Other names 2-cyano-6-phenoxypyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:501378-40-1 SDS

501378-40-1Relevant academic research and scientific papers

Nickel-Catalyzed Etherification of Phenols and Aryl Halides through Visible-Light-Induced Energy Transfer

Zhu, Da-Liang,Jiang, Shan,Wu, Qi,Wang, Hao,Li, Hai-Yan,Li, Hong-Xi

supporting information, p. 8327 - 8332 (2021/10/25)

Notwithstanding some progress in nickel-catalyzed etherification of alkanols and arylhalides, the ability of such a Ni-catalyzed transformation employing phenols to diaryl ethers is unsuccessful due to phenolates with much lower reduction potentials, which suppress the oxidation of nickel(II) intermediates into requisite Ni(III) species. We herein report visible-light-initiated, nickel-catalyzed O-arylation of phenols with arylhalides using t-BuNH(i-Pr) as the base and thioxanthen-9-one as the photosensitizer under visible light. This photocoupling exhibits a broad substrate scope.

NOVEL ANTIMALARIA AGENT CONTAINING HETEROCYCLIC COMPOUND

-

Page/Page column 70-71, (2008/06/13)

Disclosed is an antimalarial agent containing a compound represented by the formula: [wherein A1 represents a 3-pyridyl group that may have a substituent, a 6-quinolyl group that may have a substituent, or the like; X1 represents a group represented by the formula -C(=O)-NH- or the like; E represents a furyl group, a thienyl group or a phenyl group; with the proviso that A1 may have one to three substituents, and E has one of two substituents] or a salt thereof or hydrates thereof.

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