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2(1H)-Quinoxalinone,3-methyl-,4-oxide(7CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90417-40-6

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90417-40-6 Usage

Structure

Quinoxaline derivative with a methyl group at the third position and an oxide group at the fourth position.

Type

Chemical compound and derivative of quinoxalinone.

Uses

Widely used in organic synthesis and pharmaceutical applications.

Potential activities

Has potential biological and pharmacological activities.

Therapeutic applications

Being studied for its potential therapeutic applications.

Research status

The precise mechanisms and uses are still being investigated, and further research is needed to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90417-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90417-40:
(7*9)+(6*0)+(5*4)+(4*1)+(3*7)+(2*4)+(1*0)=116
116 % 10 = 6
So 90417-40-6 is a valid CAS Registry Number.

90417-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-oxido-1H-quinoxalin-4-ium-2-one

1.2 Other means of identification

Product number -
Other names 3-methyl-4-oxy-1H-quinoxalin-2-one

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:90417-40-6 SDS

90417-40-6Upstream product

90417-40-6Downstream Products

90417-40-6Relevant academic research and scientific papers

Structural elucidation of degradation products of olaquindox under stressed conditions by accurate mass measurements using electrospray ionization hybrid ion trap/time-of-flight mass spectrometry

Liu, Zhao-Ying,Zhang, Hua-Hai,Chen, Xiao-Jun,Zhou, Xiao-Ni,Wan, Leren,Sun, Zhi-Liang

experimental part, p. 90 - 96 (2012/02/14)

In this study, the stress degradation of olaquindox under conditions of hydrolysis (neutral, acidic and basic), oxidation and photolytic stress was investigated. In order to characterize each degradation product, we developed a rapid, sensitive and reliable high-performance liquid chromatography combined with hybrid ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF) method. The degradation products formed under different forced conditions were separated using an ODS-C18 column with gradient elution. Multiple scans of degradation products in MS and MS/MS modes and accurate mass measurements were performed through data-dependent acquisition. The structural elucidations of degradation products were performed by comparing the changes in the accurate molecular masses and fragment ions generated from precursor ions with those of parent drug. The present results showed that maximum degradation was observed in hydrolysis, especially in the acidic condition. The drug was also degraded significantly under photolytic conditions. A total of 12 degradation products of olaquindox were detected and characterized using the developed method. The main degradation product was formed by the complete cleavage of side chain to form 3-methyl-2-hydroxylquinoxaline-4-oxide. A degradation pathway of olaquindox was also tentatively proposed for the first time based on these characterized structures.

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