Welcome to LookChem.com Sign In|Join Free
  • or
10,10-Diphenyl-10H-phenoxasilin is a complex organic-inorganic hybrid compound, characterized by its unique structure that combines organic phenyl groups with inorganic silicon and oxygen atoms. 10,10-Diphenyl-10H-phenoxasilin is part of a class of materials known as phenoxasilins, which are of interest due to their potential applications in various fields, such as materials science and chemistry. The specific arrangement of the phenyl groups and the silicon-oxygen framework in 10,10-Diphenyl-10H-phenoxasilin contributes to its distinct chemical and physical properties. While the exact applications and properties of this particular compound may vary, phenoxasilins in general are studied for their thermal stability, optical characteristics, and potential use in the development of new materials with tailored properties.

18733-65-8

Post Buying Request

18733-65-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

18733-65-8 Usage

Chemical structure

A cyclic silanol derivative containing a silicon atom bonded to two phenyl groups and an oxygen atom.

Synonyms

Diphenylsilanol

Application

Building block in the synthesis of various organosilicon compounds.

Application

Reagent in organic chemistry reactions.

Potential pharmaceutical applications

Studied for its unique chemical properties and potential biological activity.

Potential biomedical applications

Studied for its unique chemical properties and potential biological activity.

Materials science exploration

Investigated for its potential uses in the development of specialty polymers and coatings.

Physical state

Likely a solid at room temperature, though specific information on its physical state is not provided in the material.

Solubility

Information on solubility is not provided in the material, but it may be soluble in organic solvents due to its organic components.

Check Digit Verification of cas no

The CAS Registry Mumber 18733-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,3 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18733-65:
(7*1)+(6*8)+(5*7)+(4*3)+(3*3)+(2*6)+(1*5)=128
128 % 10 = 8
So 18733-65-8 is a valid CAS Registry Number.

18733-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 10,10-diphenylphenoxasilin

1.2 Other means of identification

Product number -
Other names 10,10-diphenyl-10H-phenoxasiline

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:18733-65-8 SDS

18733-65-8Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THE SAME

-

Page/Page column 0106; 0107, (2019/02/02)

A heterocyclic compound represented by the following Formula 1 and an organic electroluminescence device including the same are provided. In Formula 1, X1 and X2 are each independently represented by any one of the following Formulae

AROMATIC COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THE SAME

-

Paragraph 0146; 0147, (2019/04/05)

An aromatic compound which improves emission efficiency and an organic electroluminescence device including the same are provided. The organic electroluminescence device includes: a first electrode; a second electrode opposite to the first electrode; and

Homogeneous hydrogenations of nitriles catalyzed by rhenium complexes

Rajesh, Kunjanpillai,Dudle, Balz,Blacque, Olivier,Berke, Heinz

supporting information; experimental part, p. 1479 - 1484 (2011/08/05)

Rhenium(I) nitrosyl complexes bearing large bite angle diphosphines efficiently catalyze the hydrogenation of nitriles to the corresponding symmetrical secondary amines. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 18733-65-8