637024-23-8

Basic information

• Product Name: 1,3-Dioxane,2-(3-methoxyphenyl)-(9CI)
• Synonyms: 1,3-Dioxane,2-(3-methoxyphenyl)-(9CI)
• CAS NO: 637024-23-8
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.22706
• Product Categories: PHENYL
• Mol File: 637024-23-8.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Dioxane,2-(3-methoxyphenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane,2-(3-methoxyphenyl)-(9CI)(637024-23-8)
• EPA Substance Registry System: 1,3-Dioxane,2-(3-methoxyphenyl)-(9CI)(637024-23-8)

Safety Data

• Hazardous Substances Data: 637024-23-8(Hazardous Substances Data)

Usage

Usage

Pharmaceutical and research industries

Physical appearance

White to light yellow crystalline powder

Melting point

157-161°C

Primary use

Intermediate in the synthesis of various pharmaceutical drugs and research compounds

Safety

Handle with care and follow safety protocols due to potential hazards

Upstream product

• 591-31-1 3-methoxy-benzaldehyde 
• 504-63-2 trimethyleneglycol 
• 59276-28-7 m-anisaldehyde dimethyl acetal 

Downstream Products

• 579488-95-2 C₁₂H₁₅NO₄ 
• 1243701-31-6 C₁₆H₂₂O₄ 
• 591-31-1 3-methoxy-benzaldehyde 
• 570377-89-8 2-[1,3]dioxan-2-yl-6-methoxy-benzonitrile N-oxide 

Relevant articles and documents

Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I

A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.

Total synthesis of the antibiotic BE-43472B

Total control: The antibiotic BE-43472B with a unique bisanthraquinone structure has been synthesized in a completely stereocontrolled manner. The key steps are 1) a pinacol rearrangement to install the angular naphthyl group, 2) a diastereoselective methylation of a lactol derivative, and 3) the late-stage installation of the labile hydroxy group through an epoxide. Copyright

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.