70952-62-4 Usage
Uses
Used in Pharmaceutical Industry:
3,6-Dichloro-4-methoxypyridazine is used as an intermediate in the synthesis of pharmaceuticals for its ability to act as a building block in the preparation of various organic compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3,6-Dichloro-4-methoxypyridazine serves as an intermediate in the synthesis of agrochemicals, contributing to the development of new pesticides or other agricultural chemicals that can improve crop protection and yield.
Used in Organic Synthesis:
3,6-Dichloro-4-methoxypyridazine is also used as a building block in the preparation of other organic compounds, enabling the synthesis of a wide range of chemical products with various applications in different industries. Its versatility in organic synthesis makes it a valuable component in the development of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 70952-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,5 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70952-62:
(7*7)+(6*0)+(5*9)+(4*5)+(3*2)+(2*6)+(1*2)=134
134 % 10 = 4
So 70952-62-4 is a valid CAS Registry Number.
70952-62-4Relevant academic research and scientific papers
HETEROARYL SUBSTITUTED 3-(1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
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Page/Page column 340-341, (2022/02/15)
The present disclosure provides a compound of Formula (I): (I), or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Rx and X1 are as defined herein, and methods of making and using same.
Access to 4-alkylaminopyridazine derivatives via nitrogen-assisted regioselective pd-catalyzed reactions
Blaise, Emilie,Kümmerle, Arthur E.,Hammoud, Hassan,De Arajo-Jnior, Jo Xavier,Bihel, Frdric,Bourguignon, Jean-Jacques,Schmitt, Martine
, p. 10311 - 10322 (2015/02/19)
3-Substituted, 6-substituted, and unsymmetrical 3,6-disubstituted 4-alkylaminopyridazines were prepared from a sequence of three chemo- and regioselective reactions combining amination and palladium-catalyzed cross-coupling reactions, such as reductive dehalogenation and Suzuki-Miyaura reactions. Extension of the methodology to Sonogashira reaction yielded a novel class of 3-substituted pyrrolopyridazines.
