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40296-46-6

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40296-46-6 Usage

Uses

Different sources of media describe the Uses of 40296-46-6 differently. You can refer to the following data:
1. Ethyl 4,6-Dichloronicotinate acts as a reactant in the preparation of (acylamino)aminonaphthyridinones as novobiocin analogs and Hsp90 inhibitors, their antitumor activities in human breast cancer cell lines, and the effects on aptoptosis and cell cycle advancement of selected compounds.
2. Ethyl 4,6-dichloronicotinate, is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as a fine chemical intermediate.

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 40296-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40296-46:
(7*4)+(6*0)+(5*2)+(4*9)+(3*6)+(2*4)+(1*6)=106
106 % 10 = 6
So 40296-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NO2/c1-2-13-8(12)5-4-11-7(10)3-6(5)9/h3-4H,2H2,1H3

40296-46-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H63092)  Ethyl 4,6-dichloronicotinate, 95%   

  • 40296-46-6

  • 250mg

  • 188.0CNY

  • Detail
  • Alfa Aesar

  • (H63092)  Ethyl 4,6-dichloronicotinate, 95%   

  • 40296-46-6

  • 1g

  • 564.0CNY

  • Detail
  • Alfa Aesar

  • (H63092)  Ethyl 4,6-dichloronicotinate, 95%   

  • 40296-46-6

  • 5g

  • 2254.0CNY

  • Detail

40296-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4,6-Dichloronicotinate

1.2 Other means of identification

Product number -
Other names Ethyl 4,6-Dichloropyridine-3-carboxylate

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:40296-46-6 SDS

40296-46-6Relevant articles and documents

Design, synthesis and anti-HIV evaluation of novel diarylnicotinamide derivatives (DANAs) targeting the entrance channel of the NNRTI binding pocket through structure-guided molecular hybridization

Liu, Zhaoqiang,Chen, Wenmin,Zhan, Peng,De Clercq, Erik,Pannecouque, Christophe,Liu, Xinyong

, p. 52 - 62 (2014)

Through a structure-based molecular hybridization approach, a novel series of diarylnicotinamide derivatives (DANAs) targeting the entrance channel of HIV-1 NNRTIs binding pocket (NNIBP) were rationally designed, synthesized and evaluated for their anti-H

Novel approach towards 3,7-disubstituted 1,6-naphthyridin-4(1H)-ones exploiting cross-coupling and SNAr reactions of a dihalogenated compound

Dembélé, Ousmane,Montoir, David,Yvorra, Thomas,Sérillon, Dylan,Tonnerre, Alain,Duflos, Muriel,Robert, Jean-Michel,Bazin, Marc-Antoine

, p. 3519 - 3523 (2018/08/24)

A new route towards the synthesis of a series of 3,7-disubstituted 1,6-naphthyridin-4(1H)-ones in moderate to good yields is reported. The strategy involves the preparation of a 3,7-dihalogenated compound that undergoes differential functionalization using palladium-catalyzed cross-coupling and SNAr reactions.

Bicyclic heterocyclic anthranilic diamides as ryanodine receptor modulators with insecticidal activity

Jeanguenat, André,Durieux, Patricia,Edmunds, Andrew J.F.,Hall, Roger G.,Hughes, Dave,Loiseleur, Olivier,Pabba, Jagadish,Stoller, André,Trah, Stephan,Wenger, Jean,Dutton, Anna,Crossthwaite, Andrew

, p. 403 - 427 (2016/01/25)

The diamide insecticides act on the ryanodine receptor (RyR). The synthesis of various bicyclic anthranilic derivatives is reported. Their activity against the insect ryanodine receptor (RyR) and their insecticidal activity in the greenhouse is presented,

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