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4-Methylpyridazine

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4-Methylpyridazine Basic information

Product Name:
4-Methylpyridazine
Synonyms:
  • 4-METHYLPYRIDAZINE
  • 4-METHYLPYRADIZINE
  • 4-METHYLPYRIDAZINE 97%
  • Pyridazine, 4-Methyl-
  • 4-Methylpyridazin-3-aMine
  • 4-Methyl-1,2-diazine
  • 4-Methylpyridazine,97%
  • 4-Methylpyridazine>
CAS:
1120-88-3
MF:
C5H6N2
MW:
94.11
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyridazines
Mol File:
1120-88-3.mol
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4-Methylpyridazine Chemical Properties

Boiling point:
98-100 °C/11 mmHg (lit.)
Density 
1.06 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.521(lit.)
Flash point:
222 °F
storage temp. 
Sealed in dry,Room Temperature
pka
3.74±0.10(Predicted)
form 
Liquid
color 
Clear yellow
Specific Gravity
1.060
λmax
292nm(H2O)(lit.)
BRN 
105689
InChI
InChI=1S/C5H6N2/c1-5-2-3-6-7-4-5/h2-4H,1H3
InChIKey
AIKUBOPKWKZULG-UHFFFAOYSA-N
SMILES
C1=NN=CC=C1C
CAS DataBase Reference
1120-88-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36
WGK Germany 
3
HS Code 
29339900

MSDS

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4-Methylpyridazine Usage And Synthesis

Chemical Properties

Clear yellow liquid

Uses

4-Methylpyridazine was used in the preparation of series of novel pyridazine derivatives structurally related to bipyridine cardiotonics.

Reactions

4-methylpyridazine could be used as a starting material to synthesize a series of novel pyridazine derivatives structurally related to bipyridine cardiotonics[1].
Pyridazine (pydz) and 4-methylpyridazine (4Me-pydz) could form stable bis(monodentate) complexes of general formulae fac-[PtXMe3L2](X = Cl, Br or I) and fac-[ReX(CO)3L2](X = Cl, Br or I). These complexes in above-ambient temperature solutions exhibit 1,2-fluxional shifts between the nitrogen donor pairs of each ring[2].

General Description

Products of reaction of methyl iodide with 4-methylpyridazine has been investigated by NMR spectra. Solvent free oxidation of 4-methylpyridazine by acetyl peroxyborate, peracetic acid and hydrogen peroxide has been reported.

References

[1] Haider N, et al. Pyridazine analogues of biologically active compounds. Part 5: Novel potential cardiotonics of the amrinone type. Organic Electronics, 1989.
[2] Abel E, et al. 1,2-Metallotropic shifts in trimethylplatinum(IV) and tricarbonylrhenium(I) halide complexes of pyridazine and 4-methylpyridazine. Journal of the Chemical Society, Dalton Transactions, 1994; 445-455.

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