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N-(2-methoxyethyl)-3-nitropyridin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

866010-53-9

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866010-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866010-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,0,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 866010-53:
(8*8)+(7*6)+(6*6)+(5*0)+(4*1)+(3*0)+(2*5)+(1*3)=159
159 % 10 = 9
So 866010-53-9 is a valid CAS Registry Number.

866010-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Methoxyethyl)-3-nitro-2-pyridinamine

1.2 Other means of identification

Product number -
Other names N-[2-(methyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]cyclopropanesulfonamide

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:866010-53-9 SDS

866010-53-9Relevant academic research and scientific papers

IMIDAZOLYL-IMIDAZOLES AS KINASE INHIBITORS

-

Page/Page column 72, (2011/10/13)

Disclosed are compounds having the formula: wherein R1A, R1B, R2 and R3 are as defined herein, and methods of making and using the same.

Preparation of 1-alkyl-2-aryl-1H-imidazo[4,5-b]pyridines from 2-alkylamino-3-aminopyridines and aromatic aldehydes using air as an oxidant

Krasavin, Mikhail,Kobak, Vladimir V.,Bondarenko, Tatiana Y.,Kravchenko, Dmitry V.

, p. 2189 - 2194 (2007/10/03)

Attempted imine formation between 2-methoxyethylamino-3-aminopyridine (an exemplary 2-alkylamino-3-aminopyridine) and an array of aromatic aldehydes in methanol and ambient atmosphere led to the predominant formation of 1-methoxyethyl-2-aryl-1H-imidazo[4,

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