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2-BroMoMethylquinoxaline 1,4-Dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18080-66-5

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18080-66-5 Usage

Chemical Properties

Red Solid

Uses

Antimicrobial activity.

Check Digit Verification of cas no

The CAS Registry Mumber 18080-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18080-66:
(7*1)+(6*8)+(5*0)+(4*8)+(3*0)+(2*6)+(1*6)=105
105 % 10 = 5
So 18080-66-5 is a valid CAS Registry Number.

18080-66-5SDS

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 2-Bromomethylquinoxaline 1,4-Dioxide

1.2 Other means of identification

Product number -
Other names 3-(bromomethyl)-4-oxidoquinoxalin-1-ium 1-oxide

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:18080-66-5 SDS

18080-66-5Relevant academic research and scientific papers

Esters of quinoxaline-1,4-dioxides

-

, (2008/06/13)

Disclosed herein are novel esters of quinoxaline-1,4-dioxide of the structure SPC1 In which X is selected from the group consisting of a single bond, lower n-alkylene and --(CH2)p --CH=CH--(CH2)q -- where p and q may have integral values from zero to four with the proviso that p+q is less than or equal to four; A is selected from the group consisting of hydrogen, hydroxyl, lower alkyl, lower alkoxy, fluorine, chlorine, bromine, iodine, cyano and trifluoromethyl; And R is selected from the group consisting of hydrogen, lower alkanoyl and α-hydroxy lower alkyl. When administered to animals, these compounds function as antibacterial agents, promote growth and improve feed efficiency. They are particularly useful in the prophylaxis and treatment of pasturellosis and salmonellosis and are notable for their extremely low toxicity in the test animal.

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