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70593-56-5

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70593-56-5 Usage

General Description

2,4-Dichloronicotinamide is a chemical compound with the molecular formula C6H4Cl2N2O. It is a derivative of nicotinamide and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2,4-Dichloronicotinamide has been studied for its potential use as a herbicide and plant growth regulator due to its ability to disrupt the biosynthesis of auxins, plant hormones essential for growth and development. In addition to its agricultural applications, 2,4-Dichloronicotinamide is also being researched for its potential to inhibit the growth of cancer cells and bacteria. It is important to handle and use 2,4-Dichloronicotinamide with care, as it is toxic if ingested or inhaled and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 70593-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,9 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70593-56:
(7*7)+(6*0)+(5*5)+(4*9)+(3*3)+(2*5)+(1*6)=135
135 % 10 = 5
So 70593-56-5 is a valid CAS Registry Number.

70593-56-5SDS

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 2,4-dichloro-nicotinic acid amide

1.2 Other means of identification

Product number -
Other names 2,4-DICHLOROPYRIDINE-3-CARBOXAMIDE

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:70593-56-5 SDS

70593-56-5Downstream Products

70593-56-5Relevant articles and documents

Identification of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted kinase inhibitors

Dai, Yujia,Hartandi, Kresna,Soni, Niru B.,Pease, Lori J.,Reuter, David R.,Olson, Amanda M.,Osterling, Donald J.,Doktor, Stella Z.,Albert, Daniel H.,Bouska, Jennifer J.,Glaser, Keith B.,Marcotte, Patrick A.,Stewart, Kent D.,Davidsen, Steven K.,Michaelides, Michael R.

, p. 386 - 390 (2008/04/03)

Tumor angiogenesis is mediated by KDR and other VEGFR and PDGFR kinases. Their inhibition presents an attractive approach for developing anticancer therapeutics. Here, we report a series of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted k

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