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2-Ethyl-6-phenylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59239-12-2

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59239-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59239-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,3 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59239-12:
(7*5)+(6*9)+(5*2)+(4*3)+(3*9)+(2*1)+(1*2)=142
142 % 10 = 2
So 59239-12-2 is a valid CAS Registry Number.

59239-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl-6-phenylpyridine

1.2 Other means of identification

Product number -
Other names 2-ethyl-6-phenyl-pyridine

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:59239-12-2 SDS

59239-12-2Downstream Products

59239-12-2Relevant academic research and scientific papers

Visible-light- And bromide-mediated photoredox Minisci alkylation of N-heteroarenes with ester acetates

Deng, Guo-Jun,Huang, Huawen,Shi, Hang,Wang, Chunlian

supporting information, p. 9177 - 9181 (2021/11/16)

A visible-light-induced photoredox Minisci alkylation reaction of N-heteroarenes with ethyl acetate has been reported. The low-toxic ethyl acetate was used for the first time as an alkylation reagent. Hence, 4-quinazolinones, quinolines and pyridines reacted smoothly in the current reaction system. Mechanistic studies indicate that LiBr plays a key role to dramatically improve the efficiency of the reaction by the mediation of hydrogen atom transfer. This journal is

Rare-earth-catalyzed C-H bond addition of pyridines to olefins

Guan, Bing-Tao,Hou, Zhaomin

supporting information; experimental part, p. 18086 - 18089 (2012/01/03)

An efficient and general protocol for the ortho-alkylation of pyridines via C-H addition to olefins has been developed, using cationic half-sandwich rare-earth catalysts, which provides an atom-economical method for the synthesis of alkylated pyridine der

Thermal characterization of the solid state and raw material fluconazole by thermal analysis and pyrolysis coupled to GC/MS

Moura, Elisana Afonso,Correia, Lidiane Pinto,Pinto, Marcia Ferraz,Procopio, Jose Valdilanio Virgulino,De Souza, Fabio Santos,MacEdo, Rui Oliveira

body text, p. 289 - 293 (2010/08/04)

This article had studied the thermal characterization of the raw material and different fluconazole crystals, obtained through recrystallization with different solvents using thermoanalytical techniques (TG, DTA, DSC-50, DSC Photovisual, DSC-60) and Pyr-GC/MS. The results confirmed that the fluconazole volatilizes without decomposition until 250 °C. Pyr-GC/MS showed hexachlorobenzene like impurities in fluconazole raw material.

REGIOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED PYRIDINES VIA GRIGNARD ADDITION TO 1-(ALKOXYCARBOXY)-PYRIDINIUM SALTS

Webb, Thomas R.

, p. 3191 - 3194 (2007/10/02)

A regioselective one pot synthesis of 2-substituted pyridine derivatives from pyridine-1-oxides is described.

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