19533-07-4

Basic information

• Product Name: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone
• CAS NO: 19533-07-4
• Molecular Formula: C₁₆H₁₄O₃
• Molecular Weight: 254.2806
• Mol File: 19533-07-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 415.5°C at 760 mmHg
• Flash Point: 196.8°C
• Density: 1.2g/cm³
• Vapor Pressure: 4.12E-07mmHg at 25°C
• Refractive Index: 1.59
• CAS DataBase Reference: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(19533-07-4)
• EPA Substance Registry System: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(19533-07-4)

Safety Data

• Hazardous Substances Data: 19533-07-4(Hazardous Substances Data)

Usage

General Description

The chemical "[4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone" is a compound with the molecular formula C17H14O3. It is a ketone with two phenyl groups attached to a central methanone group, and an oxiran-2-ylmethoxy group attached to one of the phenyl rings. [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone is commonly used as a building block in organic synthesis and pharmaceutical research. It may also have potential applications in the development of new materials and drug molecules. The unique structure of this compound makes it an interesting target for further study and exploration in various scientific fields.

Upstream product

• 1137-42-4 4-Hydroxybenzophenone 
• 106-89-8 epichlorohydrin 

Downstream Products

• 1228572-53-9 C₆₃H₉₉NO₁₈Si₈ 
• 1228572-62-0 C₆₂H₁₀₅NO₂₀Si₈ 
• 1228572-52-8 C₆₁H₁₁₁NO₂₂Si₈ 
• 1228572-59-5 C₅₇H₁₀₃NO₂₀Si₈ 
• 1228572-63-1 C₆₀H₁₀₁NO₁₉Si₈ 
• 1228572-61-9 C₈₁H₁₁₈N₂O₂₁Si₈ 
• 1263192-76-2 C₇₀H₇₂N₂O₁₂ 
• 1263192-81-9 C₆₈H₆₈N₂O₁₃ 
• 1263192-77-3 C₇₀H₇₂N₂O₁₄ 
• 700854-58-6 [4-(2-hydroxy-3-piperidine-1-ylpropoxy)phenyl]phenylmethanone 
• 701219-37-6 [4-(2-hydroxy-3-morpholine-4-ylpropoxy)phenyl]phenylmethanone 
• 825607-19-0 {4-[2-hydroxy-3-(4-(o-tolyl)piperazine-1-yl)propoxy]phenyl}phenylmethanone 
• 868212-95-7 (4-{3-[4-(4-fluorophenyl)piperazine-1-yl]-2-hydroxypropoxy}phenyl)phenylmethanone 
• 825607-20-3 (4-{3-[4-(2,3-xylyl)piperazine-1-yl]-2-hydroxypropoxy}phenyl)phenylmethanone 

Relevant articles and documents

Synthesis and characterization of polymerizable one-component photoinitiator based on sesamol

Migration stability and biocompatibility are the crucial features for a photoinitiator or coinitiator used in UV curable formulations, especially when the cured product is in direct contact with food or human skin. To reduce the migration issues and increase the biocompatibility, a polymerizable one-component photoinitiator, 1-(1,3-benzodioxol-5-yloxy)-3-(4-benzoylphenoxy) propan-2-yl acrylate (BDOBPAc), based on sesamol and benzophenone has been synthesized. The photopolymerization induced by BDOBPAc was monitored by real-time infrared spectroscopy. The rate of decomposition and the migration stability of photoinitiators were studied by UV-Vis spectroscopy. The results showed that BDOBPAc is an effective free radical photoinitiator with good migration stability, which has great potential to be widely used in the food packing or biomedical fields.

Discovery of (phenoxy-2-hydroxypropyl)piperidines as a novel class of voltage-gated sodium channel 1.7 inhibitors

A novel class of NaV1.7 inhibitors has been identified by high-throughput screening followed by structure activity relationship studies. Among this series of compounds, piperidine 9o showed potent human and mouse NaV1.7 inhibitory activities with fair subtype selectivity over NaV1.5. Compound 9o successfully demonstrated analgesic efficacy in mice comparable to that of the currently used drug, mexiletine, but with an expanded central nervous system safety margin.

Photocrosslinked hydrogel blend surface coatings

Hydrogel polymer blends including precursors and crosslinked forms of the compositions. The blends provide an improved approach to achieve high quality, uniform coatings with better commercial viability than other approaches including copolymerization. Applications include mass spectral analysis of biomolecular analytes such as proteins. Dextran and acrylamide systems are preferred. Benzophenone groups can be used as photocrosslinking groups. Photoinitiators are not needed. Functionalities which can selectively bind to biomolecular analytes are included.