5663-30-9

Basic information

• Product Name: 2-phenethyl-1,3-dioxane
• Synonyms: 2-phenethyl-1,3-dioxane
• CAS NO: 5663-30-9
• Molecular Formula: C₁₂H₁₆O₂
• Molecular Weight: 192.25
• Mol File: 5663-30-9.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 286.3°Cat760mmHg
• Flash Point: 133.9°C
• Appearance: /
• Density: 1.029g/cm³
• Vapor Pressure: 0.00458mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: 2-phenethyl-1,3-dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenethyl-1,3-dioxane(5663-30-9)
• EPA Substance Registry System: 2-phenethyl-1,3-dioxane(5663-30-9)

Safety Data

• Hazardous Substances Data: 5663-30-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H16O2/c1-2-5-11(6-3-1)7-8-12-13-9-4-10-14-12/h1-3,5-6,12H,4,7-10H2

Upstream product

• 108-86-1 bromobenzene 
• 79148-55-3 2-(2-iodoethyl)-1,3-dioxane 
• 33884-43-4 2-(2-Bromoethyl)-1,3-dioxane 
• 100-47-0 benzonitrile 
• 623-26-7 terephthalonitrile 
• 104-53-0 3-phenyl-propionaldehyde 
• 30076-98-3 (3,3-dimethoxypropyl)benzene 
• 504-63-2 trimethyleneglycol 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 200435-90-1 3-(cinnamyloxy)propan-1-ol 
• 23418-91-9 9-phenyl-9-borabicyclo[3.3.1]nonane 
• 100-59-4 phenylmagnesium chloride 

Downstream Products

• 107728-80-3 3-hydroxypropyl 3-phenylpropanoate 
• 289053-74-3 1-iodo-5-(2-phenylethyl)-4-oxa-6-heptyne 
• 1003852-69-4 3-(1-phenethylprop-2-ynyloxy)propyl p-toluenesulfonate 
• 1003852-68-3 3-(1-phenethylprop-2-ynyloxy)propan-1-ol 

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.

Synthesis of oxacyclic scaffolds via dual ruthenium hydride/Bronsted acid-catalyzed isomerization/cyclization of allylic ethers

A ruthenium hydride/Bronsted acid-catalyzed tandem sequence is reported for the synthesis of 1,3,4,9-tetrahydropyrano[3,4-b]indoles (THPIs) and related oxacyclic scaffolds. The process was designed on the premise that readily available allylic ethers would undergo sequential isomerization, first to enol ethers (Ru catalysis), then to oxocarbenium ions (Bronsted acid catalysis) amenable to endo cyclization with tethered nucleophiles. This methodology provides not only an attractive alternative to the traditional oxa-Pictet-Spengler reaction for the synthesis of THPIs, but also convenient access to THPI congeners and other important oxacycles such as acetals.

Copper nanoparticle-catalyzed cross-coupling of alkyl halides with Grignard reagents

A cross-coupling reaction between alkyl bromides and chlorides and various Grignard reagents was carried out in the presence of commercially available copper or copper oxide nanoparticles as a catalyst and an alkyne additive. The catalytic system shows high activity, a broad scope, and good functional group tolerance.