92208-10-1

Basic information

• Product Name: 1,3-Dioxane, 2-methyl-2-(2-phenylethyl)-
• CAS NO: 92208-10-1
• Molecular Formula: C13H18O2
• Molecular Weight: 206.285
• Mol File: 92208-10-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxane, 2-methyl-2-(2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane, 2-methyl-2-(2-phenylethyl)-(92208-10-1)
• EPA Substance Registry System: 1,3-Dioxane, 2-methyl-2-(2-phenylethyl)-(92208-10-1)

Safety Data

• Hazardous Substances Data: 92208-10-1(Hazardous Substances Data)

Upstream product

• 17642-78-3 2-methyl-2-phenethyl-[1,3]oxathiolane 
• 504-63-2 trimethyleneglycol 
• 39854-49-4 2-methyl-2-(2-phenylethyl)-1,3-dithiane 
• 17887-80-8 1,3-bis(trimethylsiloxy)propane 
• 2550-26-7 4-Phenyl-2-butanone 

Downstream Products

• 39854-49-4 2-methyl-2-(2-phenylethyl)-1,3-dithiane 
• 2550-26-7 4-Phenyl-2-butanone 

Relevant articles and documents

Iodine-catalyzed, efficient and mild procedure for highly chemoselective acetalization of carbonyl compounds under neutral aprotic conditions

Various types of carbonyl compounds are efficiently converted to their 1,3-dioxanes by the use of 1,3-bis(trimethylsiloxy)propane (BTSP) and a catalytic amount of iodine (3-7 mol%) under essentially neutral aprotic condition.

Highly efficient and chemoselective interchange of 1,3-oxathioacetals and dithioacetals to acetals promoted by N-halosuccinimide

Highly efficient interconversion of a range of 1,3-oxathiolanes, 1,3-dithiolanes and 1,3-dithianes to their acetals at ambient temperature using N-bromosuccinimide or N-chlorosuccinimide and different types of alcohols and diols was investigated.

Efficient and chemoselective conversion of carbonyl compounds to 1,3-dioxanes catalyzed with N-bromosuccinimide under almost neutral reaction conditions

(formula presented) Various types of carbonyl compounds were converted to the corresponding 1,3-dioxanes in the presence of ethyl orthoformate, 1,3-propanediol, and a catalytic amount of NBS via an in situ acetal exchange process. In contrast to conventional acid-catalyzed acetalization reactions, acid-sensitive substrates such as THP ethers and TBDMS ethers remain intact under described reaction conditions.