107228-53-5 Usage
General Description
3,6-dichloro-4,5-diethylpyridazine is a specialized chemical compound belonging to the group of pyridazines and its derivatives. Pyridazines are aromatic organic compounds characterized by a six-membered ring structure with two nitrogen atoms and four carbon atoms. In the compound 3,6-dichloro-4,5-diethylpyridazine, these base pyridazine molecules are further substituted with two chlorine and two ethyl groups. The compound has potential use in chemistry, pharmacology, or materials science, such as in the synthesis of various pharmaceuticals or the creation of new materials. However, its precise characteristics and potential uses need further investigation and academic research. It should be handled with care due to its potentially reactive nature and potential health risks associated with exposure or improper handling.
Check Digit Verification of cas no
The CAS Registry Mumber 107228-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,2 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107228-53:
(8*1)+(7*0)+(6*7)+(5*2)+(4*2)+(3*8)+(2*5)+(1*3)=105
105 % 10 = 5
So 107228-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10Cl2N2/c1-3-5-6(4-2)8(10)12-11-7(5)9/h3-4H2,1-2H3
107228-53-5Relevant articles and documents
TRIAZOLOPYRIDAZINES AS PAR1 INHIBITORS, PRODUCTION THEREOF, AND USE AS MEDICAMENTS
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Page/Page column 54, (2011/02/26)
The invention relates to novel compounds of formula I where R1, R2, R3, R4, R5, R6, R7, R8, Q1, Q2 and Q3 are each as defined below. The compounds of formula I have antithrombotic activity and inhibit especially protease-activated receptor 1 (PAR1). The i
Preparation of substituted pyridazines
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, (2008/06/13)
A novel process is described for preparing substituted pyridazines, where a less substituted pyridazine is reacted with a carboxylic acid in the presence of a silver ion as catalyst, using peroxydisulfate ion. The reaction is run at a temperature from about 40° to 80° C. in an aqueous solvent system and mineral acid. The substituted pyridazines are useful as intermediates to herbicidal and fungicidal compounds.
