Pyridazine, 98+%
Pyridazine, 98+%
Pyridazine, 98+%
Thermo Scientific Chemicals

Pyridazine, 98+%

CAS: 289-80-5 | C4H4N2 | 80.09 g/mol
製品番号(カタログ番号) A13266.06
または、製品番号A13266-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS289-80-5
IUPAC Namepyridazine
Molecular FormulaC4H4N2
InChI KeyPBMFSQRYOILNGV-UHFFFAOYSA-N
SMILESC1=CC=NN=C1
さらに表示
Appearance (Color)Clear colorless to yellow to brown
Assay (GC)≥98.0%
Refractive Index1.5220-1.5260 @ 20?C
FormLiquid
Pyrrolo[1,2-b]pyridazine 1 is a N-bridgehead aromatic heterocycle containing two nitrogen atoms, is obtained by the condensation of pyridazine and pyrrole.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Pyrrolo[1,2-b]pyridazine 1 is a N-bridgehead aromatic heterocycle containing two nitrogen atoms, is obtained by the condensation of pyridazine and pyrrole.

Solubility
Miscible with water, benzene, DMF. Soluble in alcohol, ether

Notes
Store at room temperature. Incompatible with oxidizing agents. Air sensitive.
RUO – Research Use Only

General References:

  1. A Chetouani.;A Aouniti.; B Hammouti.; N Benchat.; T Benhadda.; S Kertit. Corrosion inhibitors for iron in hydrochloride acid solution by newly synthesised pyridazine derivatives.Corros. Sci. 2003, 45 (8),1675-1684 .
  2. Udo Beckmann.; Sally Brooker. Cobalt(II) complexes of pyridazine or triazole containing ligands: spin-state control. Coord. Chem. Rev. 2003, 245 (1-2), .
  3. Reacts with Grignard reagents by 1,4-addition to give 4-substituted 1,4-dihydropyridazines in moderate yield: Acta Chem. Scand., 44, 279 (1990).