2568-24-3

Basic information

• Product Name: 4,7-DIHYDRO-2-PHENYL-1,3-DIOXEPIN
• Synonyms: 4,7-DIHYDRO-2-PHENYL-1,3-DIOXEPIN;4 7-DIHYDRO-2-PHENYL-1 3-DIOXEPIN 98%;4,7-Dihyro-2-phenyl-1,3-dioxepin;2-Phenyl-4,7-dihydro-1,3-dioxepin;2-phenyl-4,7-dihydro-1,3-dioxepine
• CAS NO: 2568-24-3
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.21
• Mol File: 2568-24-3.mol
• Article Data: 13

Chemical Properties

• Melting Point: 75-76 °C(Solv: hexane (110-54-3))
• Boiling Point: 114 °C/3.5 mmHg(lit.)
• Flash Point: 113 °C
• Appearance: /
• Density: 1.11 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00772mmHg at 25°C
• Refractive Index: n20/D 1.543(lit.)
• CAS DataBase Reference: 4,7-DIHYDRO-2-PHENYL-1,3-DIOXEPIN(CAS DataBase Reference)
• NIST Chemistry Reference: 4,7-DIHYDRO-2-PHENYL-1,3-DIOXEPIN(2568-24-3)
• EPA Substance Registry System: 4,7-DIHYDRO-2-PHENYL-1,3-DIOXEPIN(2568-24-3)

Safety Data

• Hazardous Substances Data: 2568-24-3(Hazardous Substances Data)

Usage

General Description

4,7-Dihydro-2-Phenyl-1,3-Dioxepin is a chemical compound that is categorized under the class of organic cyclic compounds known as dioxepins. In general, Dioxepins are compounds obtaining a dioxepine ring, which is a six-member saturated heterocycle that has two oxygen atoms and four carbon atoms. While there is limited information about this specific molecule's properties and applications, dioxepins are generally known for their utility in organic chemistry as versatile intermediates in various chemical synthesis processes. Information relating to the safety, toxicity or environmental hazards of 4,7-Dihydro-2-Phenyl-1,3-Dioxepin is not fully available.

InChI:InChI=1/C11H12O2/c1-2-6-10(7-3-1)11-12-8-4-5-9-13-11/h1-7,11H,8-9H2

Upstream product

• 100-52-7 benzaldehyde 
• 821-11-4 1,4-butenediol 
• 6117-80-2 1,4-butenediol 

Downstream Products

• 651325-74-5 (1R,4S,7S)-8,8-Dichloro-4-phenyl-3,5-dioxa-bicyclo[5.1.0]octane 
• 23829-08-5 (1R,4R,7S)-8,8-Dichloro-4-phenyl-3,5-dioxa-bicyclo[5.1.0]octane 
• 96502-55-5 (E)-1-benzyloxy-2-hexene-4,6-diol 
• 96502-54-4 methyl (E)-6-benzyloxy-3-hydroxy-4-hexenoate 
• 96502-56-6 (E)-1-benzyloxy-6-tert-butyldimethylsilyloxy-2-hexen-4-ol 
• 96502-76-0 (9S,9aR)-9-Benzyloxymethyl-5,7-dimethoxy-6-methyl-9,9a-dihydro-3H-pyrrolo[1,2-a]indol-8-ol 
• 96502-75-9 (+/-)-(9R^*,9aS^*)-8-acetoxy-9-<(benzyloxy)methyl>-9,9-dihydro-5,7-dimethoxy-6-methyl-3H-pyrrolo<1,2-a>indole 
• 96502-57-7 (E)-1-benzyloxy-6-tert-butyldimethylsilyloxy-4-<(2,4-dimethoxy-3-methylphenyl)oxy>-2-hexene 
• 96502-86-2 Acetic acid (9S,9aR)-9-benzyloxymethyl-5,7-dimethoxy-6-methyl-4-oxy-9,9a-dihydro-3H-pyrrolo[1,2-a]indol-8-yl ester 
• 96502-58-8 [(E)-6-Benzyloxy-5-(2,4-dimethoxy-3-methyl-phenoxy)-hex-3-enyloxy]-tert-butyl-dimethyl-silane 
• 96502-66-8 Acetic acid 3-amino-2-((E)-1-benzyloxymethyl-5-hydroxy-pent-2-enyl)-4,6-dimethoxy-5-methyl-phenyl ester 
• 96502-68-0 Acetic acid 3-amino-2-((E)-1-benzyloxymethyl-5-bromo-pent-2-enyl)-4,6-dimethoxy-5-methyl-phenyl ester 
• 96502-62-4 Acetic acid 6-[(E)-1-benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enyl]-2,4-dimethoxy-3-methyl-phenyl ester 
• 96502-73-7 Acetic acid (1R,9S,9aS)-9-benzyloxymethyl-5,7-dimethoxy-6-methyl-1-phenylselanyl-2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indol-8-yl ester 

Relevant articles and documents

Degradable precision polynorbornenes via ring-opening metathesis polymerization

In an attempt to introduce monomer sequence control in a growing polynorbornene via ring-opening metathesis polymerization, we employ dioxepins to efficiently determine the location of the monomers on the macromolecule backbone. Owing to the acid-labile a

Monofunctional metathesis polymers via sacrificial diblock copolymers

(Chemical Equation Presented) A small price to pay: The second block of a diblock copolymer is "sacrificed" in order to leave behind a monofunctionalized metathesis polymer with a hydroxy end group. By incorporation of a dioxepine unit into the copolymer, a breaking point is created between the block to be end-functionalized and the block to be sacrificed.

Lewis Acid-Catalyzed Vinyl Acetal Rearrangement of 4,5-Dihydro-1,3-dioxepines: Stereoselective Synthesis of cis- And trans-2,3-Disubstituted Tetrahydrofurans

Lewis acid-catalyzed rearrangements of 4,5-dihydro-1,3-dioxepines have been investigated. Rearrangement of vinyl acetals under a variety of conditions resulted in cis- and trans-2,3-disubstituted tetrahydrofuran derivatives in a highly stereoselective man