41105-99-1

Basic information

• Product Name: Phenol, 2-[(methyloxidoimino)methyl]-
• CAS NO: 41105-99-1
• Molecular Formula: C8H9NO2
• Molecular Weight: 151.165
• Mol File: 41105-99-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[(methyloxidoimino)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[(methyloxidoimino)methyl]-(41105-99-1)
• EPA Substance Registry System: Phenol, 2-[(methyloxidoimino)methyl]-(41105-99-1)

Safety Data

• Hazardous Substances Data: 41105-99-1(Hazardous Substances Data)

Upstream product

• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 90-02-8 salicylaldehyde 
• 180265-66-1 2-((hydroxy(methyl)amino)methyl)phenol 
• 89-95-2 2-methyl-benzyl alcohol 

Downstream Products

• 180265-66-1 2-((hydroxy(methyl)amino)methyl)phenol 
• 85835-91-2 8-methyl-6,6-diphenyl-5,7-dioxa-8-azonia-6-borata-6,7-dihydro-5H-benzocycloheptene 
• 71-36-3 butan-1-ol 

Relevant articles and documents

Synthesis and application of phenyl Nitrone derivatives as acidic and microbial corrosion inhibitors

Nitrone has drawn great attention due to its wide applications as a 1,3-dipole in heterocyclic compounds synthesis and the bioactivities. With the special structure, nitrone can also be used as ligand in inorganic chemistry. Based on the current research,

An efficient and rapid chemoselective synthesis of α-Aryl-N-methylnitrones in dry media

A simple, efficient, and eco-friendly procedure was developed for the condensation of N-methylhydroxylamine hydrochloride with benzaldehydes bearing electron-donating or electron-withdrawing substituents in the presence of powdered molecular sieves (3 A)

Nitrogen inversion and N-O bond rotation processes in di- and tri-substituted hydroxylamines. A dynamic NMR study

The barriers to inversion in several acyclic di- and tri-substituted hydroxylamines are determined by 1H NMR band shape analysis.The barriers range from 49.1 to 66.8 kJ mol1- and are discussed in terms of a conformational process which involves nitrogen inversion and rotation around the N-O bond.The N-benzyl group with an ortho hydroxy substituent increases the nitrogen inversion barrier by 10 kJ mol-1, which indicates the requirement of breaking of the intramolecular hydrogen bond prior to inversion.