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4-AMino-5-nitronicotinaMide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

911461-18-2

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911461-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911461-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,4,6 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 911461-18:
(8*9)+(7*1)+(6*1)+(5*4)+(4*6)+(3*1)+(2*1)+(1*8)=142
142 % 10 = 2
So 911461-18-2 is a valid CAS Registry Number.
InChI:InChI=1S/C6H6N4O3/c7-5-3(6(8)11)1-9-2-4(5)10(12)13/h1-2H,(H2,7,9)(H2,8,11)

911461-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-5-nitropyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 4-Amino-5-nitronicotinamide

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:911461-18-2 SDS

911461-18-2Downstream Products

911461-18-2Relevant academic research and scientific papers

Design, synthesis and biological evaluation of novel imidazo[4,5-c] pyridinecarboxamide derivatives as PARP-1 inhibitors

Zhu, Qihua,Wang, Xuyan,Chu, Zhaoxing,He, Guangwei,Dong, Guangping,Xu, Yungen

, p. 1993 - 1996 (2013/04/24)

A series of novel cyclic amine-substituted imidazo[4,5-c] pyridinecarboxamide analogs were designed and synthesized. All the target compounds were evaluated for their PARP inhibition activity, and the result indicated that most of the compounds possessed

Transformations of ortho-methoxyaryl(hetaryl)carboxamides into quinazolin-4-one and pyrido[2,3-d]pyrimidin-4-one derivatives

Ryabova,Makarov,Alekseeva,Shashhov,Chernyshev,Granik

, p. 1907 - 1914 (2007/10/03)

ortho-Chloroaryl(hetaryl)carboxamides containing one or two nitro groups at positions 3 and/or 5 of the ring undergo condensation accompanied by the pyrimidine ring closure on refluxing in an excess of sodium methoxide to form bicyclic products, viz., qui

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