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328379-53-9

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328379-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328379-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,3,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 328379-53:
(8*3)+(7*2)+(6*8)+(5*3)+(4*7)+(3*9)+(2*5)+(1*3)=169
169 % 10 = 9
So 328379-53-9 is a valid CAS Registry Number.

328379-53-9SDS

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 fluoro-(2,3,4,5,6-pentafluorophenyl)xenon

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:328379-53-9 SDS

328379-53-9Relevant 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.

Bis(pentafluorophenyl)xenon, Xe(C6F5)2: A homoleptic diorganoxenon derivative

Maggiarosa, Nicola,Naumann, Dieter,Tyrra, Wieland

, p. 4588 - 4591 (2007/10/03)

A step forward in organo xenon chemistry: The fluoride-initiated reaction of Me3SiC6F5 and XeF2 leads, via the intermediate C6F5XeF, to an isolable [10-Xe-2] species with two xenon-carbon bonds (see scheme).

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