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151099-09-1

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151099-09-1 Usage

Class

Naphthyridine derivatives

Core structure

Naphthyridine

Substitution pattern

Ethoxy group at the 6-position and a methyl group at the 7-position

Type of molecule

Heterocyclic

Potential applications

Pharmacological and biological activities

Relevance

Medicinal chemistry and drug discovery

Status

Potential candidate for developing new therapeutic agents

Research needs

Further research to explore properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 151099-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,9 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151099-09:
(8*1)+(7*5)+(6*1)+(5*0)+(4*9)+(3*9)+(2*0)+(1*9)=121
121 % 10 = 1
So 151099-09-1 is a valid CAS Registry Number.

151099-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethoxy-7-methyl-1,8-naphthyridin-4-ol

1.2 Other means of identification

Product number -
Other names 6-ethoxy-6H-1,2-oxazine-3-carbaldehyde

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:151099-09-1 SDS

151099-09-1Downstream Products

151099-09-1Relevant articles and documents

Condensed 4-aminopyridines with antirheumatic activity

-

, (2008/06/13)

Compounds of formula I STR1 and pharmaceutically acceptable salts thereof in which one of A or B represents N and the other represents N or C--R3 ; R1 represents hydrogen, halo, alkyl, hydroxy, carboxyalkenyl, alkoxycarbonylalkenyl, hydroxyalkyl, carboxyalkyl, alkoxycarbonylalkyl, alkoxy, halogenated alkyl, carboxy, alkoxycarbonyl, alkanoylamino or carbamoylalkenyl; R2 represents hydrogen, alkyl, halo, alkoxy, hydroxy, alkanoyloxy, or phenoxy; R3 represents hydrogen or alkyl; R4 represents hydrogen, halo, alkoxycarbonyl, cyano, benzyloxycarbonyl, alkanoyl, benzoyl, alkyl, carboxy, alkylthio or carbamoyl; R5 represents hydrogen or alkyl; R9 represents hydrogen or alkyl; R10 represents phenyl, pyridyl or pyrimidinyl substituted by OR6 and optionally further substituted wherein R6 represents hydrogen, alkyl, alkoxycarbonyl or carbamoyl, alicyclic hydrocarbon, phenyl, cycloalkylalkyl, arylalkyl or pyridyl; or when R10 represents phenyl, OR6 represents a monosaccharide group or a disaccharide group; which are antirheumatic agents. Compositions containing these compounds and processes to prepare them are also disclosed.

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