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64500-19-2

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64500-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64500-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,0 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64500-19:
(7*6)+(6*4)+(5*5)+(4*0)+(3*0)+(2*1)+(1*9)=102
102 % 10 = 2
So 64500-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O2/c1-6(13)4-9(14)12-8-3-2-7(10)5-11-8/h2-3,5H,4H2,1H3,(H,11,12,14)

64500-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-chloro-2-pyridyl)-3-oxobutanamide

1.2 Other means of identification

Product number -
Other names -

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:64500-19-2 SDS

64500-19-2Relevant articles and documents

Facile synthesis and antibacterial, antitubercular, and anticancer activities of novel 1,4-dihydropyridines

Sirisha, Kalam,Achaiah, Garlapati,Reddy, Vanga Malla

experimental part, p. 342 - 352 (2011/07/30)

A series of twenty new 4-substituted-2,6-dimethyl-3,5-bis-N-(heteroaryl)- carbamoyl-1,4-dihydropyridines have been prepared from a three-component one-pot condensation reaction of N-heteroaryl acetoacetamide, an aromatic/ heteroaromatic aldehyde, and ammonium acetate under four different experimental conditions. Except for the conventional method, all the experimental conditions were simple, eco-friendly, economical, and the reactions were rapid and high-yielding. The methods employed have been compared in terms of yields, cost, and simplicity. The synthesized compounds were characterized by different spectroscopic techniques and evaluated for their in-vitro anticancer, antibacterial, and antitubercular activities. Amongst the compounds tested, compound 25 exhibited the highest anticancer activity while compounds 14 and 18 exhibited significant antibacterial and antitubercular activities.

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