29040-48-0

Basic information

• Product Name: 6-METHOXY-2-METHYLBENZOFURAN
• Synonyms: 6-METHOXY-2-METHYLBENZOFURAN;BENZOFURAN, 6-METHOXY-2-METHYL-;6-methoxy-2-methyl-1-benzofuran;6-METHOXY-2-METHYLBENZOFURAN(WXG01732)
• CAS NO: 29040-48-0
• Molecular Formula: C₁₀H₁₀O₂
• Molecular Weight: 162.19
• Mol File: 29040-48-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 122 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.106±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-METHOXY-2-METHYLBENZOFURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 6-METHOXY-2-METHYLBENZOFURAN(29040-48-0)
• EPA Substance Registry System: 6-METHOXY-2-METHYLBENZOFURAN(29040-48-0)

Safety Data

• Hazardous Substances Data: 29040-48-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 30, p. 1867, 1989 DOI: 10.1016/S0040-4039(00)99601-1

Upstream product

• 122-84-9 4-methoxybenzyl methyl ketone 
• 97946-21-9 Acetone O-(m-methoxyphenyl)oxime 
• 41580-72-7 m-methoxyphenyl 2-propynyl ether 
• 37592-19-1 3-allyloxyanisole 
• 678554-43-3 C₁₅H₁₆N₂O₄S 
• 41046-70-2 2-iodo-5-methoxyphenol 
• 74-99-7 prop-1-yne 
• 150-19-6 O-methylresorcine 

Downstream Products

• 54584-24-6 6-hydroxy-2-methylbenzofuran 
• 638217-07-9 6-methoxy-2-methylbenzofuran-3-carboxylic acid methylamide 

Relevant articles and documents

A ONE STEP SYNTHESIS OF 2-SUBSTITUTED BENZOFURANS FROM 2-ARYL-1-SUBSTITUTED ETHANE-1-ONES BY PHOTOINDUCED SET REACTIONS

An efficient one step synthesis of 2-substituted Benzofurans from the enolate of 2-Aryl-1-substituted ethane-1-ones by photoinduced SET has been reported.

Direct Synthesis of 2-Methylbenzofurans from Calcium Carbide and Salicylaldehyde p -Tosylhydrazones

A new methodology for the construction of methyl-substituted benzofuran rings from the reactions of calcium carbide with salicylaldehyde p-tosylhydrazones/2-hydroxyacetophenone p-tosylhydrazones is described. Various 2-methylbenzofurans and 2,3-dimethylbenzofurans could be obtained in satisfactory yield by using a cuprous chloride catalyst. The advantages of this protocol include the use of a readily available and easy-to-handle acetylene source and simple workup procedure.

NOVEL QUINOLINE DERIVATIVES

The invention relates to compounds represented by Formula (I): and to pharmaceutically acceptable salts or solvates of said compounds, wherein each of A, R3-8, X3, X5, m, and n are defined herein. The invention also relates to pharmaceutical compositions containing the compounds of Formula (I) and to methods of treating hyperproliferative disorders in a mammal by administering compounds of Formula (I).

Benzofused heterozryl amide derivatives of thienopyridines useful as therapeutic agents, pharmaceutical compositions including the same, and methods for their use

The invention relates to compounds represented by the formula I and to prodrugs or metabolites thereof, or pharmaceutically acceptable salts or solvates of said compounds, said prodrugs, and said metabolites, wherein Z, Y, R11 and R14, R15, R16, and R17 are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.