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2-Quinoxalinecarboxaldehyde,6-methyl-(6CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99361-22-5

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99361-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99361-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,6 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99361-22:
(7*9)+(6*9)+(5*3)+(4*6)+(3*1)+(2*2)+(1*2)=165
165 % 10 = 5
So 99361-22-5 is a valid CAS Registry Number.

99361-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methylquinoxaline-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-Methyl-quinoxaline-2-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:99361-22-5 SDS

99361-22-5Downstream Products

99361-22-5Relevant academic research and scientific papers

Design, synthesis and biological evaluation of novel non-azole derivatives as potential antifungal agents

Tang, Hui,Wu, Juan,Zhang, Wen,Zhao, Lei,Zhang, Ya-Hui,Shen, Cheng-Wu

, p. 1161 - 1164 (2015)

A series of 3-substituted quinazolinones, 2-substituted quinoxalines and 2-substituted benzopyrans were synthesized and evaluated for their antifungal activity in vitro. The new compounds revealed excellent in vitro antifungal activity with broad spectrum. The structure-activity relationships (SARs) of the derivatives were analyzed. Compound 9A2 exhibits better antifungal activity against 5 tested fungi in vitro than fluconazole, especially against Trichophyton rubrum and Microsporum gypseum. This study provides a series of novel lead compounds for the development of non-azole antifungal agents.

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