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686-70-4

Silane, diethylfluoro-, also known as diethylfluorosilane or (diethylamino)(fluoro)silane, is a colorless, volatile, and flammable liquid with the chemical formula C4H11FNSi. It is an organosilicon compound that is used as a precursor in the synthesis of various organosilicon compounds and as a silylating agent in organic synthesis. Diethylfluoro-silane is highly reactive and can form strong Si-O bonds, making it useful in the preparation of silyl ethers and other organosilicon derivatives. Due to its reactivity, it is essential to handle Silane, diethylfluoro- with caution, using appropriate safety measures and equipment.

686-70-4

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686-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 686-70-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 686-70:
(5*6)+(4*8)+(3*6)+(2*7)+(1*0)=94
94 % 10 = 4
So 686-70-4 is a valid CAS Registry Number.

686-70-4SDS

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 diethyl(fluoro)silane

1.2 Other means of identification

Product number -
Other names Diaethylfluorsilan

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:686-70-4 SDS

686-70-4Downstream Products

686-70-4Relevant articles and documents

C6F5XeY Molecules (Y = F and Cl): New synthetic approaches. first structural proof of the organoxenon halide molecule C 6F5XeF

Bilir, Vural,Frohn, Hermann-Josef

, p. 505 - 512 (2013/09/23)

The arylxenonium salt [C6F5Xe][BF4] reacts with different sources of nucleophiles, Y (naked fluoride, [N(CH 3)4]F, the silanes, (CH3)3SiCl and (C2H5)3SiH, and the cadmiumorganyl, Cd(C 6F5)2), in coordinating solvents (C 2H5CN, CH3CN, CD3CN). While the products C6F5XeF, C6F5XeCl, and (C6F5)2Xe are well defined molecules, in reactions with (C2H5)3SiH only decomposition products presumably derived from 6F5XeH6F5XeC2H56F5XeF are discussed.

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