23639-82-9

Basic information

• Product Name: Phenol, 4-(1,3-dioxolan-2-yl)-
• CAS NO: 23639-82-9
• Molecular Formula: C9H10O3
• Molecular Weight: 166.177
• Mol File: 23639-82-9.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Phenol, 4-(1,3-dioxolan-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-(1,3-dioxolan-2-yl)-(23639-82-9)
• EPA Substance Registry System: Phenol, 4-(1,3-dioxolan-2-yl)-(23639-82-9)

Safety Data

• Hazardous Substances Data: 23639-82-9(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 107-21-1 ethylene glycol 

Downstream Products

• 77924-21-1 5-(4-[1,3]Dioxolan-2-yl-phenoxy)-1-phenyl-1H-tetrazole 
• 123-08-0 4-hydroxy-benzaldehyde 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 57529-05-2 4-(1,3-dithian-2-yl)phenol 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 54730-30-2 4-hydroxy-3-C-prenylbenzaldehyde 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 1448638-99-0 2-(4-(methoxymethoxy)phenyl)-1,3-dioxolane 

Relevant articles and documents

A facile and efficient protocol for esterification and acetalization in a PEG1000-D(A)IL/toluene thermoregulated catalyst-media combined systems

A novel efficient and recyclable temperature-dependent biphasic catalyst and reaction media combined system comprised of PEG-1000 linked dicationic acidic ionic liquid and toluene was developed and applied in esterification of aromatic acids and acetalization of aromatic aldehydes with good to excellent yields. This system is characteristic of temperature-dependent reversible biphasic property, simple and facile recyclability, high catalytic activity and extensive substrate and reaction adaptability.

Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions

Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.

Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds

Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds was also demonstrated. The advantages of the polyaniline-sulfate salt are ease of preparation and handling, stability, reusability and activity.