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Pyridinium, 1-(triphenylmethyl)-, tetrakis(pentafluorophenyl)borate(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

675827-04-0

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675827-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 675827-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,8,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 675827-04:
(8*6)+(7*7)+(6*5)+(5*8)+(4*2)+(3*7)+(2*0)+(1*4)=200
200 % 10 = 0
So 675827-04-0 is a valid CAS Registry Number.

675827-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tritylpyridinium tetrakis(pentafluorophenyl)borate

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:675827-04-0 SDS

675827-04-0Upstream product

675827-04-0Relevant articles and documents

Chiral Memory in Silyl-Pyridinium and Quinolinium Cations

Fernandes, Anthony,Laye, Claire,Pramanik, Suman,Palmeira, Dayvson,Pekel, ?zgen ?mür,Massip, Stéphane,Schmidtmann, Marc,Müller, Thomas,Robert, Frédéric,Landais, Yannick

, p. 564 - 572 (2020)

Pyridine- and quinoline-stabilized silyl cations have been prepared, and their structure in condensed phases unambiguously assigned using 1H, 13C, 15N, 29Si, and 1H DOSY NMR as well as X-ray diffraction studies. Solid state structures thus show in both cases a stabilization of the cationic silicon center through an N-Si interaction and formation of a highly strained four-membered ring system. Chiral memory at the silicon atom in these heterocycle-stabilized silyl cations was also established, leading to various levels of selectivity depending on the nature of the heterocycle. Lowest energy conformations of the starting silanes obtained through DFT calculations, along with the isolation and characterization of the Si-centered chiral silyl cation intermediates, finally allowed to propose a plausible hypothesis as to the configurational stability of these silyl cations.

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