60582-30-1

Basic information

• Product Name: Phenol, 2-(dimethoxymethyl)-6-methoxy-
• CAS NO: 60582-30-1
• Molecular Formula: C10H14O4
• Molecular Weight: 198.219
• Mol File: 60582-30-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenol, 2-(dimethoxymethyl)-6-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-(dimethoxymethyl)-6-methoxy-(60582-30-1)
• EPA Substance Registry System: Phenol, 2-(dimethoxymethyl)-6-methoxy-(60582-30-1)

Safety Data

• Hazardous Substances Data: 60582-30-1(Hazardous Substances Data)

Upstream product

• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 149-73-5 trimethyl orthoformate 
• 67-56-1 methanol 
• 7150-01-8 2-acetoxy-3-methoxybenzaldehyde 

Downstream Products

• 1352089-60-1 C₁₅H₁₂O₆ 
• 1352089-64-5 C₁₅H₁₄O₆ 

Relevant articles and documents

Selective synthesis of 4,6-O-alkenylidene and -benzylidene acetals from unprotected sucrose by lanthanide(III) resin-catalyzed transacetalization

Lanthanide cation exchanged resins were used as catalysts for the acetalization of sucrose. Ytterbium(III)- and erbium(III)-exchanged resins promote the transacetalization of dialkyl acetals of α,β-unsaturated aldehydes. A two-step one-pot procedure provides direct access from the unsaturated aldehyde to a series of sucrose 4,6-acetals in good yields from unprotected sucrose without concomitant glycosidic bond cleavage.

Acetal Formation Facilitated in 2-Hydroxyaryl Aldehydes by Intramoleculedar Acyl Group Transfer

Convenient preparations of synthetically useful acetals, a dithioacetal and an oxathiolan from the 2-acyl derivatives of 2-hydroxyaryl aldehydes under basic conditions are described.The mildness of the reaction conditions is illustrated by the formation of an ethoxycarbonyl-substituted dioxolan.The reaction is dependent upon an intramolecular acetyl group transfer and the mechanism of the reaction is discussed.Some broader implications of this type of acyl transfer are discussed.