10410-28-3

Basic information

• Product Name: 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL-
• Synonyms: 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL-;6-METHOXY-3-METHYL-2-BENZOFURANCARBOXALDEHYDE;6-Methoxy-3-methyl-benzofuran-2-carbaldehyde
• CAS NO: 10410-28-3
• Molecular Formula: C11H10O3
• Molecular Weight: 190.2
• Mol File: 10410-28-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL-(10410-28-3)
• EPA Substance Registry System: 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL-(10410-28-3)

Safety Data

• Hazardous Substances Data: 10410-28-3(Hazardous Substances Data)

Usage

General Description

2-Benzofurancarboxaldehyde, 6-Methoxy-3-Methyl- is a chemical compound with a molecular formula C11H10O3 and a molecular weight of 190.2 g/mol. It is a white to light yellow powder with a melting point of 101-104°C and a boiling point of 295.7°C. 2-BENZOFURANCARBOXALDEHYDE, 6-METHOXY-3-METHYL- is commonly used in the synthesis of pharmaceuticals, perfumes, and other organic products. It is also known for its fruity and floral odor, making it a popular choice in the fragrance industry. Additionally, it is used in research and development as a building block for the synthesis of various organic compounds. Overall, 2-Benzofurancarboxaldehyde, 6-Methoxy-3-Methyl- is a versatile and valuable chemical with a wide range of applications.

Upstream product

• 29040-52-6 6-methoxy-3-methylbenzofuran 
• 74-90-8 hydrogen cyanide 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 53724-96-2 ethyl 6-methoxy-3-methylbenzofuran-2-carboxylate 
• 6437-63-4 1-(3-methoxyphenoxy)propan-2-one 
• 150-19-6 O-methylresorcine 

Downstream Products

• 10410-29-4 6-methoxy-3-methyl-benzofuran-2-carboxylic acid 

Relevant articles and documents

Efficient synthesis of chiral benzofuryl β-amino alcohols via a catalytic asymmetric Henry reaction

Chiral β-amino alcohol ligands were found effective for the copper(ii)-catalyzed asymmetric Henry reaction of benzofuran-2-carbaldehydes with nitromethane, which led to the formation of (S)-enriched benzofuryl β-nitro alcohols with satisfactory enantioselectivities (up to 98% ee). Using this catalytic protocol, bioactive (S)-benzofuryl β-amino alcohols could be conveniently prepared in short steps.

Efficient and connective assembly of highly functionalized benzofurans using o-hydroxyphenones and dichloroethylene

The preparation of highly functionalized benzofurans by a unique and connective transformation is reported. Base-catalyzed condensation of o-hydroxyphenones with 1,1-dichloroethylene generates the corresponding chloromethylene furans. These labile intermediates undergo a facile rearrangement into benzofuran carbaldehydes under mild acidic conditions.