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"Benzene, (diethoxyfluorosilyl)-" is a chemical compound with the molecular formula C10H15FOSi. It is an organosilicon compound, which means it contains silicon along with carbon and hydrogen atoms. This specific compound features a benzene ring, a six-carbon aromatic ring, with a diethoxyfluorosilyl group attached to it. The diethoxyfluorosilyl group consists of a silicon atom bonded to a fluorine atom and two ethoxy groups (each ethoxy group being an ethyl group with an oxygen atom attached). benzene, (diethoxyfluorosilyl)- is used in the synthesis of various organosilicon materials and can be found in applications such as silicones, adhesives, and sealants. Due to its reactivity and the presence of the fluorine atom, it can also be used in the preparation of other organosilicon compounds with specific properties.

310-39-4

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310-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 310-39-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 310-39:
(5*3)+(4*1)+(3*0)+(2*3)+(1*9)=34
34 % 10 = 4
So 310-39-4 is a valid CAS Registry Number.

310-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diethoxy-fluoro-phenylsilane

1.2 Other means of identification

Product number -
Other names Diaethoxy-fluor-phenyl-silan

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:310-39-4 SDS

310-39-4Downstream Products

310-39-4Relevant academic research and scientific papers

Cleavage of the C-Si bond in trifluoro(phenyl)silane with aliphatic alcohols

Voronkov,Boyarkina,Gebel',Albanov,Basenko

, p. 1927 - 1929 (2008/02/03)

Trifluoro(phenyl)silane reacts with aliphatic alcohols under reflux. The reaction involves not only Si-F bond cleavage to form ethoxyfluoro(phenyl) silanes, but also C-Si bond cleavage to form benzene and alkoxyfluoro- and tetraalkoxysilanes. The formation of the latter products was proved by 19F and 29Si NMR spectroscopy and also by model disproportionation reactions of trifluoro(phenyl)silane with trimethoxy-(phenyl)-, tetramethoxy-, or tetraethoxysilanes.

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