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1120-88-3

1120-88-3 Structure

1120-88-3 Structure
IdentificationMore
[Name]

4-Methylpyridazine
[CAS]

1120-88-3
[Synonyms]

4-METHYLPYRADIZINE
4-METHYLPYRIDAZINE
4-METHYLPYRIDAZINE 97%
[Molecular Formula]

C5H6N2
[MDL Number]

MFCD00011594
[Molecular Weight]

94.11
[MOL File]

1120-88-3.mol
Chemical PropertiesBack Directory
[Appearance]

Clear yellow liquid
[Boiling point ]

98-100 °C/11 mmHg (lit.)
[density ]

1.06 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.521(lit.)
[Fp ]

222 °F
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Liquid
[pka]

3.74±0.10(Predicted)
[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 DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[HS Code ]

29339900
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

4-Methylpyridazine(1120-88-3)1HNMR
4-Methylpyridazine(1120-88-3)Raman
4-Methylpyridazine(1120-88-3)FT-IR
4-Methylpyridazine(1120-88-3)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-Methylpyridazine, 97%(1120-88-3)
[Alfa Aesar]

4-Methylpyridazine, 99%(1120-88-3)
[Sigma Aldrich]

1120-88-3(sigmaaldrich)
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