51424-04-5

Basic information

• Product Name: 2(1H)-Pyridinone,3,3'-(phenylmethylene)bis[4-hydroxy-6-methyl-
• Synonyms: NSC 288510
• CAS NO: 51424-04-5
• Molecular Formula: C19H18 N2 O4
• Molecular Weight: 338.363
• Mol File: 51424-04-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(1H)-Pyridinone,3,3'-(phenylmethylene)bis[4-hydroxy-6-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyridinone,3,3'-(phenylmethylene)bis[4-hydroxy-6-methyl-(51424-04-5)
• EPA Substance Registry System: 2(1H)-Pyridinone,3,3'-(phenylmethylene)bis[4-hydroxy-6-methyl-(51424-04-5)

Safety Data

• Hazardous Substances Data: 51424-04-5(Hazardous Substances Data)

Usage

Chemical structure

A chemical compound that contains a pyridinone ring, a phenylmethylene group, and two hydroxy-methyl groups.

Derivative of pyridinone

It is a modified version of the pyridinone compound.

Contains a phenylmethylene group

A benzene ring connected to a methylene group (-CH2-) in the chemical structure.

Contains hydroxy-methyl groups

A methyl group (-CH3) connected to an oxygen atom (-O-) in the chemical structure.

Potential applications

This compound has potential uses in the pharmaceutical and chemical industries, materials science, and biochemistry.

Synthesis of pharmaceutical drugs

It could be used to create new drugs with unique chemical properties.

Building block for designing new compounds

It can be used as a starting material for creating new compounds with enhanced biological activities.

Further research and development needed

More studies are required to fully understand and exploit the potential of this compound in various fields.

Upstream product

• 3749-51-7 4-hydroxy-6-methyl-2-pyridone 
• 40219-06-5 benzylidenecyanothioacetamide 
• 100-52-7 benzaldehyde 
• 675-10-5 4-hydroxy-6-methyl-2-pyron 
• 16929-83-2 4,4'-dihydroxy-6,6'-dimethyl-3,3'-(phenylmethylene)bis(pyran)-2,2'-dione 
• 2025-40-3 ethyl benzylidenecyanoacetate 
• 193888-02-7 ethyl 2-amino-5,6-dihydro-7-methyl-5-oxo-4-phenyl-4H-pyrano[3,2-c]pyridine-3-carboxylate 
• 193887-94-4 2-amino-5,6-dihydro-7-methyl-5-oxo-4-phenyl-4H-pyrano[3,2-c]pyridine-3-carbonitrile 

Relevant articles and documents

Synthesis of Fused 2Н-Pyridin-2-ones under the Conditions of Multicomponent Hantzsch Reaction

One-pot process was studied between a substituted 4-hydroxy-2Н-pyran-2-one and aromatic aldehydes and ammonium acetate in the conditions of modified Hantzsch reaction in acid environment under thermal and microwave activation. Arylmethylenebis-4-hydroxy-2

Synthesis and phytotoxic activity of new pyridones derived from 4-hydroxy-6-methylpyridin-2(1H)-one

Commercial dehydroacetic acid was converted into 4-hydroxy-6-methylpyridin- 2(1 H)-one (3), which was then condensed with several aliphatic aldehydes to produce seven new title compounds in variable yields (35-92%). Reaction of 3 with α,β-unsaturated aldehydes resulted in the formation of condensed pyran derivatives 4g′ and 4h′. A mechanism is proposed to explain the formation of such compounds. The effects of all methylpyridin-2(1 H)-one derivatives on the development of the dicotyledonous species Ipomoea grandifolia and Cucumis sativus and the monocotyledonous species Sorghum bicolor were evaluated. At the dose of 6.7 × 10-8 mol a.i./g substrate the compounds showed some phytotoxic selectivity, being more active against the dicotyledonous species. These compounds can be used as lead structures for the development of more active phytotoxic products.