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10536-62-6

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10536-62-6 Usage

General Description

BIS(PENTAFLUOROPHENYL)DIMETHYLSILANE is a chemical compound with the molecular formula C16H10F10Si. It is a silane compound that is used in various industrial applications, including as a precursor in the production of silicon-based materials and as a reagent in organic synthesis. It is a colorless liquid with a high boiling point, and it is highly reactive due to the presence of the pentafluorophenyl groups, which makes it a valuable reagent in organic chemistry. BIS(PENTAFLUOROPHENYL)DIMETHYLSILANE is also known for its stability and compatibility with other organic compounds, making it a versatile and useful chemical in various industrial and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 10536-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,3 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10536-62:
(7*1)+(6*0)+(5*5)+(4*3)+(3*6)+(2*6)+(1*2)=76
76 % 10 = 6
So 10536-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H6F10Si/c1-25(2,13-9(21)5(17)3(15)6(18)10(13)22)14-11(23)7(19)4(16)8(20)12(14)24/h1-2H3

10536-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(perfluorophenyl)dimethylsilane

1.2 Other means of identification

Product number -
Other names dimethyl-bis(2,3,4,5,6-pentafluorophenyl)silane

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:10536-62-6 SDS

10536-62-6Relevant articles and documents

REACTIONS OF POLYFLUORO AROMATIC COMPOUNDS WITH ELECTROPHILIC AGENTS IN THE PRESENCE OF TRIS(DIALKYLAMINO)PHOSPHINES. I. SYNTHESIS OF TRIALKYLSILYL(GERMYL, STANNYL, OR PLUMBYL)POLYFLUOROBENZENES

Bardin, V. V.,Pressman, L. S.,Rogoza, L. N.,Furin, G. G.

, p. 1931 - 1937 (2007/10/02)

Polyfluorophenyl bromides and iodides react with alkylhalo derivatives of silicon, germanium, tin, or lead in the presence of equimolar amounts of a tris(dialkylamino)phosphine to give polyfluorophenyl(alkyl) derivatives of the above-mentioned elements and phosphonium salts.Electron-donor substituents in position 4 of the polyfluorophenyl bromide slow down the reaction, while electron-acceptor substituents accelerate it.

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