1632-76-4 Usage
Description
3-Methylpyridazine, also known as 3-Mepydz, is a diazaaromatic compound that exhibits self-association in aqueous solutions across acidic, neutral, and basic pH levels. It is known for its ability to react with halogenotrimethylplatinum (IV) to form complexes of type fac-[PtXMe3(3-Mepydz)2] (X = Cl, Br, or I) and also reacts with bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato) copper (II) complexes. It is characterized by its clear yellow to brown liquid appearance.
Uses
Used in Pharmaceutical Industry:
3-Methylpyridazine is used as a diagnostic and therapeutic agent for cardiovascular diseases and conditions. Its ability to form complexes with certain metal compounds makes it a valuable tool in the development of treatments for various heart-related issues.
Used in Chemical Research:
As a diazaaromatic compound, 3-Methylpyridazine is utilized in chemical research for its unique reactivity with specific metal complexes. This property allows it to be a key component in the synthesis of new compounds and materials with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1632-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1632-76:
(6*1)+(5*6)+(4*3)+(3*2)+(2*7)+(1*6)=74
74 % 10 = 4
So 1632-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2/c1-5-3-2-4-6-7-5/h2-4H,1H3
1632-76-4Relevant articles and documents
PYRIDAZINES-XXXIX. N-SUBSTITUTED 1,2-DIHYDRO-1,2-DIAZINES FORMED IN HOMOLYTIC ALKOXYCARBONYLATION REACTIONS OF PYRIDAZINES
Gebauer, Martina,Heinisch, Gottfried,Loetsch, Gerhard
, p. 2449 - 2456 (2007/10/02)
Pyridazine and C-alkylpyridazines were found to yield N-ethoxycarbonyl-1,2-dihydropyridazines 1 - 6 when subjected to conditions of homolytic ethoxycarbonylation.This is the first example of an attack of a radical at the nitrogen atom of a N-heteroarene in Minisci-type reactions.
Application of Flash Vacuum Pyrolysis to the Synthesis of 1,2-Condensed Indoles
Ohsawa, Akio,Kawaguchi, Takayuki,Igeta, Hiroshi
, p. 1037 - 1040 (2007/10/02)
-
A STUDY ON THE TRANSITION STATE IN THE PHOTOOXYGENATIONS BY AROMATIC AMINE N-OXIDES
Ogawa, Yuji,Iwasaki, Shigeo,Okuda, Shigenobu
, p. 2277 - 2280 (2007/10/02)
Oxygen-atom transfer process in the photolysis of aromatic amine N-oxides was suggested to involve the primary oxygen-atom elimination from N-oxides to give "oxene" followed by its reactions with the oxygen-acceptors.
