401606-53-9

Basic information

• Product Name: 2(1H)-Pyridinone,1-(1,1-dimethylethoxy)-(9CI)
• Synonyms: 2(1H)-Pyridinone,1-(1,1-dimethylethoxy)-(9CI)
• CAS NO: 401606-53-9
• Molecular Formula: C9H13NO2
• Molecular Weight: 167.20502
• Product Categories: METHOXY
• Mol File: 401606-53-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2(1H)-Pyridinone,1-(1,1-dimethylethoxy)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyridinone,1-(1,1-dimethylethoxy)-(9CI)(401606-53-9)
• EPA Substance Registry System: 2(1H)-Pyridinone,1-(1,1-dimethylethoxy)-(9CI)(401606-53-9)

Safety Data

• Hazardous Substances Data: 401606-53-9(Hazardous Substances Data)

Usage

Classification

Pyridine derivative

Uses

Pharmaceutical and agrochemical industries, biological activities (antifungal, antibacterial, herbicidal), precursor in the synthesis of pharmaceutical compounds

Versatility

Potential applications in various fields

Upstream product

• 822-89-9 1-Hydroxy-2-pyridon 
• 507-19-7 t-butyl bromide 

Relevant articles and documents

2′-deoxyguanosine (DG) oxidation and strand-break formation in DNA by the radicals released in the photolysis of N-tert-butoxy-2-pyridone. Are tert-butoxyl or methyl radicals responsible for the photooxidative damage in aqueous media?

Chemical equation presented The photolysis of pyridone 3b (photo-Fenton reagent) in benzene releases tert-butoxyl radicals, which have been trapped by DMPO and EPR-spectrally identified. In aqueous solution, however, the fragmentation of the tert-butoxyl into methyl radicals prevails and the former radicals are of no direct consequence in the photooxidation of 2′-deoxyguanosine (dG) and pBR 322 DNA. The photooxidative damage of nucleic acids is caused by the oxyl radical species generated from the methyl radicals with oxygen.