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Borane, difluoro(undecafluoropentyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

658698-60-3

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658698-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 658698-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,8,6,9 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 658698-60:
(8*6)+(7*5)+(6*8)+(5*6)+(4*9)+(3*8)+(2*6)+(1*0)=233
233 % 10 = 3
So 658698-60-3 is a valid CAS Registry Number.

658698-60-3SDS

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 difluoro(perfluoropentyl)borane

1.2 Other means of identification

Product number -
Other names -

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:658698-60-3 SDS

658698-60-3Downstream Products

658698-60-3Relevant academic research and scientific papers

Rearrangement Reactions of the Transient Lewis Acids (CF3) 3B and (CF3)3BCF2: An Experimental and Theoretical Study

Finze, Maik,Bernhardt, Eduard,Zaehres, Manfred,Willner, Helge

, p. 490 - 505 (2004)

Short-lived (CF3)3B and (CF3) 3BCF2 are generated as intermediates by thermal dissociation of (CF3)3BCO and F-abstraction from the weak coordinating anion [B(CF3)4]-, respectively. Both Lewis acids cannot be detected because of their instability with respect to rearrangement reactions at the B-C-F moiety. A cascade of 1,2-fluorine shifts to boron followed by perfluoroalkyl group migrations and also difluorocarbene transfer reactions occur. In the gas phase, (CF 3)3B rearranges to a mixture of linear perfluoroalkyldifluoroboranes CnF2n+1BF2 (n = 2-7), while the respective reactions of (CF3)3BCF 2 result in a mixture of linear (n = 2-4) and branched monoperfluoroalkyldifluoroboranes, e.g., (C2F5)(CF 3)FCBF2. For comparison, the reactions of [CF 3BF3]- and [C2F5BF 3]- with AsF5 are studied, and the products in the case of [CF3BF3]- are BF3 and C2F5BF2 whereas in the case of [C 2F5BF3]-, C2F 5BF2 is the sole product. In contrast to reports in the literature, it is found that CF3BF2 is too unstable at room temperature to be detected. The decomposition of (CF3) 3BCO in anhydrous HF leads to a mixture of the new conjugate Bronsted-Lewis acids [H2F][(CF3)3BF] and [H2F][C2F5BF3]. All reactions are modeled by density functional calculations. The energy barriers of the transition states are low in agreement with the experimental results that (CF3)3B and (CF3)3BCF2 are short-lived intermediates. Since CF2 complexes are key intermediates in the rearrangement reactions of (CF3)3B and (CF3)3BCF2, CF2 affinities of some perfluoroalkylfluoroboranes are presented. CF2 affinities are compared to CO and F- affinities of selected boranes showing a trend in Lewis acidity, and its influence on the stability of the complexes is discussed. Fluoride ion affinities are calculated for a variety of different fluoroboranes, including perfluorocarboranes, and compared to those of the title compounds.

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