19533-07-4

• 

• Basic information

  1. Product Name: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone
  2. Synonyms:
  3. CAS NO:19533-07-4
  4. Molecular Formula: C₁₆H₁₄O₃
  5. Molecular Weight: 254.2806
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19533-07-4.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 415.5°C at 760 mmHg
  3. Flash Point: 196.8°C
  4. Appearance: N/A
  5. Density: 1.2g/cm³
  6. Vapor Pressure: 4.12E-07mmHg at 25°C
  7. Refractive Index: 1.59
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(CAS DataBase Reference)
  11. NIST Chemistry Reference: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(19533-07-4)
  12. EPA Substance Registry System: [4-(oxiran-2-ylmethoxy)phenyl](phenyl)methanone(19533-07-4)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 19533-07-4(Hazardous Substances Data)

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• SDS
• Upstream product
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• Article

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19533-07-4 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.

Check Digit Verification of cas no

The CAS Registry Mumber 19533-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,3 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19533-07:
(7*1)+(6*9)+(5*5)+(4*3)+(3*3)+(2*0)+(1*7)=114
114 % 10 = 4
So 19533-07-4 is a valid CAS Registry Number.

19533-07-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	[4-(oxiran-2-ylmethoxy)phenyl]-phenylmethanone

1.2 Other means of identification

Product number	-
Other names	4-glycidyloxy benzophenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19533-07-4 SDS

19533-07-4Upstream product

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

19533-07-4Downstream Products

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

19533-07-4Relevant articles and documents

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

Yang, Jinliang,Tang, Ruifen,Shi, Suqing,Nie, Jun

, p. 923 - 929 (2013)

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.

NOVEL POLYMERIC PHOTOINITIATORS AND PHOTOINITIATOR MONOMERS

-

Page/Page column, (2015/06/03)

The present invention provides polymeric photoinitiators being co-polymers of photoinitiator monomers and at least one further monomer, as well as photoinitiator monomers being intermediates in the preparation of such polymeric photoinitiators. Additionally, there is provided polyacrylate obtained by radical polymerization of at least one acrylate monomer (Ac) in the presence of such polymeric photoinitiators. In the photoinitiator monomers and polymeric photoinitiators, a photoinitiator moiety, a hydrolytic stable linker and two polymerisable functional groups are incorporated into the photoinitiator structure.

Photocrosslinked hydrogel blend surface coatings

-

, (2008/06/13)

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.

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