4-Methylpyridazine
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
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)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-37/39-36
- WGK Germany
- 3
- HS Code
- 29339900
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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4-Methylpyridazine(1120-88-3)Related Product Information
- Hydralazine
- Sulfachloropyridazine sodium
- Thioridazine
- 4-Methyl-2-pentanone
- Tetramethylpyrazine
- 3,6-Dihydroxy-4,5-dimethylpyridazine
- 3,6-Dichloropyridazine-4-carboxylic acid
- 4-Pyridazinecarboxylic acid
- 3,6-DICHLORO-4-METHYLPYRIDAZINE,3,6-Dichloro-5-methylpyridazine
- MINAPRINE DIHYDROCHLORIDE
- 4-METHYLPYRIDAZINE-3,6-DIOL,3,6-DIHYDROXY-4-METHYLPYRIDAZINE,3,6-DIHYDROXY-4-METHYLPYRIDAZINE (4-METHYLMALEIC HYDRAZIDE)
- 3,6-Dichloro-4,5-dimethylpyridazine
- 4,5-Dihydro-6-methylpyridazin-3(2H)-one
- 4-Methylpyridazine-3-carboxylicacid
- 4,5-Dimethylpyridazine-3,6-diol
- 5-METHYLPYRIDAZIN-3-AMINE
- 3-METHYLPYRIDAZINE
- 3-AMINO-6-METHYLPYRIDAZINE