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Silane, diethoxydifluoro-, also known as diethoxydifluorosilane or C4H10F2OSi, is an organosilicon compound characterized by the presence of a silicon atom bonded to two ethoxy groups (-OCH2CH3) and two fluorine atoms. This colorless liquid is an important precursor in the synthesis of various organosilicon compounds and is widely used in the production of silicones, silane coupling agents, and other specialty chemicals. Diethoxydifluorosilane is also employed as a cross-linking agent in the rubber and plastics industry, as well as a silylating agent in organic synthesis. Due to its reactivity, it is essential to handle Silane, diethoxydifluoro- with caution, as it can react with moisture and is sensitive to hydrolysis.

358-81-6

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358-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358-81-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 358-81:
(5*3)+(4*5)+(3*8)+(2*8)+(1*1)=76
76 % 10 = 6
So 358-81-6 is a valid CAS Registry Number.

358-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name difluorodiethoxysilane

1.2 Other means of identification

Product number -
Other names Diaethoxy-difluor-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:358-81-6 SDS

358-81-6Relevant academic research and scientific papers

Catalytic enantioselective aldol reaction to ketones

Oisaki, Kounosuke,Zhao, Dongbo,Kanai, Motomu,Shibasaki, Masakatsu

, p. 7164 - 7165 (2007/10/03)

An enantioselective aldol reaction between ketones and ketene silyl acetals is described using CuF-chiral phosphine as a catalyst. The key for high enantioselectivity was the development of a novel ligand derived from Taniaphos combined with the unique ac

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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