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107073-47-2

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107073-47-2 Usage

Type of compound

Organic compound

Uses

Antibacterial and antiprotozoal agent in veterinary medicine, used for treating infections in animals, particularly poultry and swine

Status

Banned for use in food-producing animals in many countries due to potential carcinogenicity

Carcinogenicity classification

Potential carcinogen (International Agency for Research on Cancer)

Safety precautions

Caution should be exercised when using or handling dimetridazole, and it is important to follow safety guidelines and regulations regarding its use.

Check Digit Verification of cas no

The CAS Registry Mumber 107073-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,7 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107073-47:
(8*1)+(7*0)+(6*7)+(5*0)+(4*7)+(3*3)+(2*4)+(1*7)=102
102 % 10 = 2
So 107073-47-2 is a valid CAS Registry Number.

107073-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethyl-3-methylidenequinoxalin-2-one

1.2 Other means of identification

Product number -
Other names 3-methylene-1,4-dimethyl-3-oxo-1,2,3,4-tetrahydroquinoxaline

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:107073-47-2 SDS

107073-47-2Downstream Products

107073-47-2Relevant articles and documents

DERIVATIVES OF 3,4-DIHYDRO-3-THIOXO-2-QUINOXALINYLACETIC ACID

Toman, Jaromir,Klicnar, Jiri

, p. 419 - 428 (2007/10/02)

Ethyl 3,4-dihydro-4-methyl-3-thioxo-2-quinoxalinylacetate has been prepared by thionation of the 3-oxo derivative.The mechanism is discussed of the reaction of this ester with diethylamine giving the two non-isomerizing ketimine-enamine tautomers and 1,2-

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