202931-70-2 Usage
Uses
Used in Research and Synthesis:
3,6-Dichloro-4-(4-pyridinyl)pyridazine is used as a research compound for the development and synthesis of new chemical entities. Its unique structure and properties make it a valuable component in the creation of novel molecules with potential applications in various fields.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3,6-Dichloro-4-(4-pyridinyl)pyridazine is used as a building block for the synthesis of new drug candidates. Its heterocyclic nature allows for the formation of complex molecules with potential therapeutic effects, making it a valuable asset in drug discovery and development.
Used in Chemical Synthesis:
3,6-Dichloro-4-(4-pyridinyl)pyridazine is used as a reagent in the synthesis of various organic compounds. Its ability to form stable bonds with other molecules makes it a useful intermediate in the production of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 202931-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,9,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 202931-70:
(8*2)+(7*0)+(6*2)+(5*9)+(4*3)+(3*1)+(2*7)+(1*0)=102
102 % 10 = 2
So 202931-70-2 is a valid CAS Registry Number.
202931-70-2Relevant articles and documents
NITROGEN-CONTAINING HETEROCYCLIC COMPOUND AND COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF
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, (2021/10/07)
Disclosed by the present invention are a nitrogen-containing heterocyclic compound, and a composition thereof, a preparation method therefor and an application thereof. The structure of the nitrogen-containing heterocyclic compound according to the presen
MAP KINASE MODULATORS AND USES THEREOF
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Paragraph 00209; 00292, (2014/09/29)
The invention provides for novel MAP kinase inhibitors and compositions comprising the same. In some embodiments, the MAP kinase inhibitors are p38a MAP kinase inhibitors. The invention further provides for methods for treatment of diseases comprising adm
Substituted triazolo-pyridazine derivatives as ligands for GABA receptors
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, (2008/06/13)
Substituted triazolo-pyridazine derivative compounds represented by wherein the variables are disclosed herein are selective ligands for GABA-A receptors, particularly for the α2 and/or α3 subunits.