79499-42-6

Basic information

• Product Name: 2-(4-methoxybenzyl)-1-methyl-1H-pyrrole
• Synonyms: 2-(4-methoxybenzyl)-1-methyl-1H-pyrrole
• CAS NO: 79499-42-6
• Molecular Weight: 201.268
• Mol File: 79499-42-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxybenzyl)-1-methyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxybenzyl)-1-methyl-1H-pyrrole(79499-42-6)
• EPA Substance Registry System: 2-(4-methoxybenzyl)-1-methyl-1H-pyrrole(79499-42-6)

Safety Data

• Hazardous Substances Data: 79499-42-6(Hazardous Substances Data)

Upstream product

• 1192-58-1 N-methylpyrrole aldehyde 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 96-54-8 N-Methylpyrrole 
• 2746-25-0 p-Methoxybenzyl bromide 
• 120-94-5 1-Methylpyrrolidine 
• 105-13-5 4-Methoxybenzyl alcohol 
• 696-62-8 para-iodoanisole 

Relevant articles and documents

Graphene oxide-phenalenyl composite: transition metal-free recyclable and catalytic C-H functionalization

An efficient route towards a heterogeneous transition metal-free catalytic C-H functionalization using a covalently linked graphene oxide-phenalenyl conjugate is described herein (28 examples, which include a core of some biologically relevant biaryl and hetero-biaryls). It is an environmentally benign, economical and heterogeneous platform, whose catalytic activity can easily be regenerated through a simple washing-drying technique and the catalytic activity can be retained even after 10 cycles.

METHOD FOR ESTABLISHING CC BONDS BETWEEN ELECTROPHILIC SUBSTRATES AND ? - NUCLEOPHILES IN NEUTRAL TO ALKALINE AQUEOUS OR ALCOHOLIC SOLVENTS WITHOUT USING A LEWIS OR BRONSTED ACID

The invention relates to a method for establishing carbon-carbon bonds by reacting electropohilic substrates that have a solvolysis rate kEtOH (25°C) > 10-6 s-1 and ? compounds. The method is characterized by generating the intermediary carbocations in neutral to alkaline aqueous or alcoholic solvents or solvent mixtures without using a Lewis or Br?nsted acid.

Tandem Alkylation-Reduction of 2-Acylpyrroles. Convenient One-Pot Syntheses of 2-Benzylpyrroles

Tandem alkylation-reduction of 2-acylpyrroles is described for the convenient one-pot syntheses of 2-benzylpyrroles.By this convenient procedure 2-(p-methoxybenzyl)pyrrole (2), 2-benzylpyrrole (3), 2-(p-methylbenzyl)pyrrole (4), 2-(o-methoxybenzyl)pyrrole