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104217-24-5

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104217-24-5 Usage

Uses

2-iso-BDMEQ is a metabolite of Mequindox (M225118). Mequindox (M225118) and its major metabolites have been detected in chicken muscles, chicken liver, swine muscles and swine liver by UPLC-MS/MS method.

Check Digit Verification of cas no

The CAS Registry Mumber 104217-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,1 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104217-24:
(8*1)+(7*0)+(6*4)+(5*2)+(4*1)+(3*7)+(2*2)+(1*4)=75
75 % 10 = 5
So 104217-24-5 is a valid CAS Registry Number.

104217-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methylquinoxalin-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names 2-Quinoxalinemethanol,a,3-dimethyl

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:104217-24-5 SDS

104217-24-5Downstream Products

104217-24-5Relevant articles and documents

Synthesis method of special antimicrobial growth-promoting drug 3-methyl-2-ethanol quinoxaline for animals

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Paragraph 0013; 0014; 0015, (2017/08/29)

The invention provides a synthesis method of a special antimicrobial growth-promoting drug 3-methyl-2-ethanol quinoxaline for animals. The synthesis method comprises the following steps: adding mequindox, a phase-transfer catalyst and solvent tetrahydrofuran into a reactor, stirring at room temperature, slowly adding a single reducer, reacting for 0.5-5 hours, and then performing aftertreatment to obtain the 3-methyl-2-ethanol quinoxaline. The method is short in reaction step and only needs one step; and the method has the advantages of simple operation, high efficiency, high product yield and purity and mild reaction conditions, thereby being suitable for industrial production.

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