CAS 50500-58-8

6-Chloro-2-(phenylmethyl)-3(2H)-pyridazinone

Description:

6-Chloro-2-(phenylmethyl)-3(2H)-pyridazinone is a chemical compound characterized by its pyridazinone core, which features a chlorine substituent at the 6-position and a phenylmethyl group at the 2-position. This structure contributes to its potential biological activity and makes it of interest in medicinal chemistry. The compound typically appears as a solid and may exhibit moderate solubility in organic solvents. Its molecular structure suggests that it could participate in various chemical reactions, including nucleophilic substitutions due to the presence of the chlorine atom. The phenylmethyl group may enhance lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, the compound may exhibit specific interactions with biological targets, making it a candidate for further research in therapeutic applications. Safety and handling precautions should be observed, as with any chemical substance, particularly those with halogen substituents, which can pose environmental and health risks. Overall, 6-Chloro-2-(phenylmethyl)-3(2H)-pyridazinone represents a compound of interest in both synthetic and medicinal chemistry contexts.

Formula: C₁₁H₉ClN₂O

InChI: InChI=1S/C11H9ClN2O/c12-10-6-7-11(15)14(13-10)8-9-4-2-1-3-5-9/h1-7H,8H2

InChI key: InChIKey=YPALKBBWTAXDAO-UHFFFAOYSA-N

SMILES: C(N1C(=O)C=CC(Cl)=N1)C2=CC=CC=C2

Synonyms:

• 2-Benzyl-6-chloro-2H-pyridazin-3-one
• 6-Chloro-2-(phenylmethyl)-3(2H)-pyridazinone
• 3(2H)-Pyridazinone, 6-chloro-2-(phenylmethyl)-
• 2-Benzyl-6-chloropyridazin-3(2H)-one
• 3(2H)-Pyridazinone, 2-benzyl-6-chloro-

2-Benzyl-6-chloro-2,3-dihydropyridazin-3-one

CAS: 50500-58-8

2-Benzyl-6-chloro-2,3-dihydropyridazin-3-one is a Grignard reagent that reacts with electrophiles to form organometallic compounds. It is used in organic chemistry as a nucleophilic agent in the formation of carbon–carbon bonds and other types of reactions. 2-Benzyl-6-chloro-2,3-dihydropyridazin-3-one can also be used to produce alkyl magnesium bromides from alcohols and chlorides. The transformation of 2,2'-bipyridine into 2,2'-bipyrimidine is one example of this reaction.

Formula: C₁₁H₉ClN₂O

Purity: Min. 95%

Molecular weight: 220.65 g/mol

Ref: 3D-ACA50058