114564-42-0

Basic information

• Product Name: 1,3-Dioxol-2-one, 4-phenyl-5-(phenylmethyl)-
• CAS NO: 114564-42-0
• Molecular Formula: C16H12O3
• Molecular Weight: 252.269
• Mol File: 114564-42-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxol-2-one, 4-phenyl-5-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxol-2-one, 4-phenyl-5-(phenylmethyl)-(114564-42-0)
• EPA Substance Registry System: 1,3-Dioxol-2-one, 4-phenyl-5-(phenylmethyl)-(114564-42-0)

Safety Data

• Hazardous Substances Data: 114564-42-0(Hazardous Substances Data)

Usage

Class

Dioxolane compounds

Structure

Dioxolane ring with a phenyl and phenylmethyl substituent

Usage

Building block in organic synthesis and medicinal chemistry

Pharmacological activities

Possesses potential pharmacological activities

Applications

Synthesis of pharmaceuticals, agrochemicals, and specialty chemicals

Development

Building block in the development of novel materials and chemical compounds

Safety

Handle with care, may present hazards if not properly controlled

Upstream product

• 75-44-5 phosgene 
• 23464-17-7 1,3-diphenylpropane-1,2-dione 

Relevant articles and documents

Neue Synthesen und Reaktionen ungesaettigter Heterotitanacyclen

Dicarbonyltitanocene reacts chemoselectively with difunctional carbonyl compounds such as 1,2-diketones and 1,4-diketo-2-enes, with α-ketothioketones, α-ketoimines and azodicarbonic esters and -amides to yield the corresponding, mostly new, heterotitanacycles that are capable of a lot of a useful follow-up reactions.These chelate complexes, containing three to four heteroatoms, allow the substitution of the entire titanocene fragment by carbon (formation of vinylenic carbonates and the thia-derivatives of these) or by further heteroatoms like boron or phosphorus(formation of boroles and phosphonic acid derivatives), thus retaining the cyclofunctionality.Alternatively, some of the new chelate complexes can be readily C-C-chain-lengthened via a deprotonating/alkylating sequence, leaving the metallacycle unaffected.