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1569-15-9

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1569-15-9 Usage

Description

7-amino-4-methyl-1,8-naphthyridin-2-ol is an organic compound derived from the leaves of the Rhododendron dauricum tree. It is characterized by its unique chemical structure, which includes an amino group, a methyl group, and a naphthyridin-2-ol moiety. 7-amino-4-methyl-1,8-naphthyridin-2-ol has been found to possess significant biological activities, making it a potential candidate for various applications in different industries.

Uses

Used in Pesticide Industry:
7-amino-4-methyl-1,8-naphthyridin-2-ol is used as an insecticide for its insecticidal activities. The compound has been shown to effectively control and manage various insect pests, thereby protecting crops and improving agricultural productivity. Its insecticidal properties make it a valuable addition to the arsenal of pest control agents, offering an alternative to traditional chemical pesticides.
Used in Pharmaceutical Industry:
7-amino-4-methyl-1,8-naphthyridin-2-ol is used as a potential pharmaceutical candidate for its diverse biological activities. The compound's unique chemical structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs. Its insecticidal properties could also be harnessed for the development of novel treatments for parasitic infections, offering a new approach to combating drug-resistant parasites.
Used in Chemical Research:
7-amino-4-methyl-1,8-naphthyridin-2-ol is used as a research tool in the field of organic chemistry and medicinal chemistry. The compound's unique structure and biological activities make it an interesting subject for further study, allowing researchers to explore its potential applications and optimize its properties for various uses. 7-amino-4-methyl-1,8-naphthyridin-2-ol can also serve as a starting material for the synthesis of new compounds with improved or novel biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 1569-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1569-15:
(6*1)+(5*5)+(4*6)+(3*9)+(2*1)+(1*5)=89
89 % 10 = 9
So 1569-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O/c1-5-4-8(13)12-9-6(5)2-3-7(10)11-9/h2-4H,1H3,(H3,10,11,12,13)

1569-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-amino-4-methyl-1H-1,8-naphthyridin-2-one

1.2 Other means of identification

Product number -
Other names 2-hydroxy-4-methyl-7-amino-1,8-naphthyridine

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:1569-15-9 SDS

1569-15-9Downstream Products

1569-15-9Relevant articles and documents

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Hauser,Weiss

, p. 453,458 (1949)

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Antithrombotic quinoxazolines

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, (2008/06/13)

Quinoxazolines having antithrombotic activity. Exemplary of those disclosed are: 4-{[6-(N-carboxymethyl-quinolin-8-yl-sulphonylamino)-1-methyl-2-oxo-1,2-dihydroquinoxalin-3-yl]-methyl}-benzamidine, 4-{[6-(1-(N-cyclopentyl-carboxymethylcarbonylamino)-cyclo-propyl)-1-methyl-2-oxo-1,2-dihydroquinoxalin-3-yl]-methyl}-benzamidine, and 4-{[7-(N-carboxymethylaminocarbonyl-ethylamino)-4-methyl-quinolin-2-yl]-oxo}-benzamidine.

Transition metal-naphthyridine chemical complexes

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, (2008/06/13)

New coordination complex compounds formed between first row transition metal salts and naphthyridine compounds substituted with electron donor groups at positions ortho and para to the nitrogen positions.

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