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4-Methylpyridazine

4-Methylpyridazine Structure
4-Methylpyridazine
  • CAS No.1120-88-3
  • Chemical Name:4-Methylpyridazine
  • CBNumber:CB8468011
  • Molecular Formula:C5H6N2
  • Formula Weight:94.11
  • MOL File:1120-88-3.mol
4-Methylpyridazine Property
  • 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)
  • UNSPSC Code 12352100
  • NACRES NA.22
Safety
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H315-H319-H335
  • Precautionary statements P261-P264-P271-P280-P302+P352-P305+P351+P338
4-Methylpyridazine Price More Price(2)
  • Brand: Sigma-Aldrich(India)
  • Product number: 297771
  • Product name : 4-Methylpyridazine
  • Purity: 97%
  • Packaging: 500MG
  • Price: ₹8270.3
  • Updated: 2022/06/14
  • Buy: Buy
  • Brand: TCI Chemicals (India)
  • Product number: M2343
  • Product name : 4-Methylpyridazine
  • Purity: min. 98.0 %
  • Packaging: 1G
  • Price: ₹12500
  • Updated: 2022/05/26
  • Buy: Buy

4-Methylpyridazine Chemical Properties,Usage,Production

  • 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.
4-Methylpyridazine Preparation Products And Raw materials
Raw materials
Preparation Products
4-Methylpyridazine Suppliers
Global(189)Suppliers
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4-Methylpyridazine Spectrum
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