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52208-50-1

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52208-50-1 Usage

Synthesis

The venerable Balz and Schiemann reaction is the most powerful methodology for preparing aryl fluorides. Not surprisingly, this reaction has been applied to the synthesis of fluoropyridines. Thus, 2,6-dichloro-3-fluoropyridine is readily prepared from 3-amino-2,6-dichloropyridine. The method has been applied to combinatorial synthesis on the solid phase.

Check Digit Verification of cas no

The CAS Registry Mumber 52208-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,0 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52208-50:
(7*5)+(6*2)+(5*2)+(4*0)+(3*8)+(2*5)+(1*0)=91
91 % 10 = 1
So 52208-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Cl2FN/c6-4-2-1-3(8)5(7)9-4/h1-2H

52208-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dichloro-3-fluoropyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2,6-dichloro-3-fluoro

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:52208-50-1 SDS

52208-50-1Relevant articles and documents

PREPARATION OF NEW 2-CHLORO-5-FLUORO-6-(4-PHENYL-METHYLPIPERAZINYL)-4-TRIFLUOROMETHYL-3-NICOTINIC ACID

Remuzon, Philippe,Bouzard, Daniel,Jacquet, Jean-Pierre

, p. 431 - 434 (2007/10/02)

The nicotinic acid (15), which could be a key intermediate for novel potential antibacterial 1,8-naphthyridine-3-carboxylic acid analogues, was prepared initiating with construction of the pyridine nucleus by ethyl 2-fluoroacetate and ethyl 2-trifluoroacetate.

Method for preparing 2,5-dihalo- and 2,5,6-trihalopyridines

-

, (2008/06/13)

A method for preparing 2,5-dihalo- and 2,5,6-trihalopyridines corresponding to the formula SPC1 Wherein each X independently represents chloro, fluoro or bromo and R represents hydrogen, chloro, fluoro or bromo which comprises reacting a halohydrazinopyridine of one of the formulas SPC2 With an excess of an aqueous alkali metal hydroxide in the presence of a reaction medium from the group consisting of loweralkanols of 1 to 4 carbon atoms and loweralkylglycols of 2 to 4 carbon atoms.

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