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2-Fluoro-6-dimethylaminopiridine-3- carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193481-63-9

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193481-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193481-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,8 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 193481-63:
(8*1)+(7*9)+(6*3)+(5*4)+(4*8)+(3*1)+(2*6)+(1*3)=159
159 % 10 = 9
So 193481-63-9 is a valid CAS Registry Number.

193481-63-9SDS

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-fluoro-6-dimethylaminopyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-(dimethylamino)-2-fluoropyridine-3-carboxaldehyde

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:193481-63-9 SDS

193481-63-9Relevant academic research and scientific papers

The structural proliferation of 2,6-difluoropyridine through organometallic intermediates

Schlosser, Manfred,Rausis, Thierry

, p. 1018 - 1024 (2007/10/03)

Contrary to a literature claim, 2,6-difluoropyridine-3-carboxaldehyde can be readily prepared by consecutive treatment of 2,6-difluoropyridine with lithium diisopropylamide and N,N-dimethylformamide. Regioselective displacements of fluorine from the aldehyde by nucleophiles were carried out. To demonstrate the versatility of the organometallic approach, some two dozens of further 2,6-difluoropyridine derivatives were prepared applying a combination of modern organometallic methods such as site selective hydrogen/metal and halogen/metal permutations and deprotonation-triggered heavy halogen migrations. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Synthesis of some piperazinylpyrazolo[3,4-b]pyridines as selective serotonin re-uptake inhibitors

Shutske, Gregory M.,Roehr, Joachim E.

, p. 789 - 795 (2007/10/03)

A number of 3-substituted 6-piperazinylpyrazolo[3,4-b]pyridines were synthesized from 2,6-difluoropyridine by directed ortho metallation and sequential intra- and intermolecular displacement of fluorine. Three derivatives with a cyano group in the 3-position showed activity as selective serotonin re-uptake inhibitors.

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