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Bromebric, also known as bromethalin, is a potent and highly toxic second-generation rodenticide primarily used to control rodents such as rats and mice. It works by disrupting the sodium-potassium pump in the rodent's nervous system, leading to severe neurological damage, convulsions, and eventually death. Bromethalin is a white crystalline powder that is odorless and has low solubility in water, making it a popular choice for bait stations. Due to its high toxicity, it is crucial to handle bromethalin with extreme caution and to follow proper safety guidelines to prevent accidental exposure to humans and non-target animals.

5711-40-0

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5711-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5711-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5711-40:
(6*5)+(5*7)+(4*1)+(3*1)+(2*4)+(1*0)=80
80 % 10 = 0
So 5711-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrO4/c1-16-8-4-2-7(3-5-8)11(15)9(12)6-10(13)14/h2-6H,1H3,(H,13,14)/b9-6+

5711-40-0SDS

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 (E)-3-p-Anisoyl-3-bromoacrylic acid

1.2 Other means of identification

Product number -
Other names Bromebric

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:5711-40-0 SDS

5711-40-0Relevant academic research and scientific papers

Pyridazines. XV. Synthesis of 6-aryl-5-amino-3(2H)-pyridazinones as potential platelet aggregation inhibitors

Estevez, Isabel,Ravina, Enrique,Sotelo, Eddy

, p. 1421 - 1428 (2007/10/03)

Several 3(2H)-pyridazinones with amino groups at the 5-position of the pyridazine nucleus have been prepared. The 6-aryl-5-halo-3(2H)-pyridazinones obtained from mucochloric and mucobromic acid lead to the corresponding 5- alkylamino-3(2H)-pyridazinones,

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