138469-75-7

Basic information

• Product Name: 1H-Indole, 5-methoxy-3-[(4-methoxyphenyl)methyl]-
• CAS NO: 138469-75-7
• Molecular Formula: C17H17NO2
• Molecular Weight: 267.327
• Mol File: 138469-75-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 5-methoxy-3-[(4-methoxyphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 5-methoxy-3-[(4-methoxyphenyl)methyl]-(138469-75-7)
• EPA Substance Registry System: 1H-Indole, 5-methoxy-3-[(4-methoxyphenyl)methyl]-(138469-75-7)

Safety Data

• Hazardous Substances Data: 138469-75-7(Hazardous Substances Data)

Upstream product

• 138469-66-6 2-(5-methoxy-2-nitrophenyl)-3-(4-methoxyphenyl)propionitrile 
• 1006-94-6 5-methoxylindole 
• 105-13-5 4-Methoxybenzyl alcohol 
• 89302-15-8 2-(5-methoxy-2-nitrophenyl)acetonitrile 

Relevant articles and documents

Acidic-functionalized ionic liquid as an efficient, green, and metal-free catalyst for benzylation of sulfur, nitrogen, and carbon nucleophiles to benzylic alcohols

A series of HSO4- functionalized ILs was synthesized and used as efficient, green, and metal-free catalysts for benzylation. Notably, the catalytic system has wide substrate scopes and the ionic liquid catalysts were applied to investigate three different types of nucleophiles to give the desired benzylation products with moderate to excellent yields.

THE USE OF o-NITROARYLACETONITRILES AS CARBON ACID PARTICIPANTS IN THE MITSUNOBU REACTION

The use of o-nitroarylacetonitriles as carbon acids in the Mitsunobu reaction is discussed as a method of carbon-carbon bond formation.This reaction represents a rare example of a carbon acid participating in a Mitsunobu reaction.