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6654-74-6

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6654-74-6 Usage

Chemical compound

2-amino-5-nitro-1-oxo-1,2-dihydropyridinium

Properties

Nitrogen-containing heterocyclic compound
Acidic and basic properties: Can act as both an acid and a base due to the presence of functional groups
Existence in different tautomeric forms: Can undergo tautomerization, leading to different structural isomers

Uses

Reagent in organic synthesis: Used in various organic reactions due to its reactivity
Precursor in pharmaceutical and agrochemical production: Serves as a starting material for the synthesis of drugs and agricultural chemicals

Biological activity

Anti-inflammatory properties: Studied for its potential to reduce inflammation
Antibacterial activity: Investigated for its ability to inhibit bacterial growth

Check Digit Verification of cas no

The CAS Registry Mumber 6654-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6654-74:
(6*6)+(5*6)+(4*5)+(3*4)+(2*7)+(1*4)=116
116 % 10 = 6
So 6654-74-6 is a valid CAS Registry Number.

6654-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-5-nitropyridin-2-imine

1.2 Other means of identification

Product number -
Other names 2-amino-5-nitropyridine 1-oxide

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:6654-74-6 SDS

6654-74-6Relevant articles and documents

Gold-catalyzed redox synthesis of imidazo[1,2-a]pyridines using pyridine N-oxide and alkynes

Talbot, Eric P. A.,Richardson, Melodie,McKenna, Jeffrey M.,Toste, F. Dean

supporting information, p. 687 - 691 (2014/04/03)

A mild, catalytic, atom economical synthesis of imidazo[1,2-a]pyridines has been developed: catalytic dichloro(2-pyridinecarboxylato)gold [PicAuCl 2] in the presence of an acid produces a range of imidazo[1,2-a]pyridines in good yields starting

Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof

-

Page/Page column 8, (2008/06/13)

Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and at least one N-oxides of six-membered rings with one or two nitrogen atoms keratin dyeing compound. A method for oxidative dyeing of keratin fibers, comprising applying such compositions in the presence of an oxidizing agent, for a period sufficient to develop the desired coloration.

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