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Niobium, tetrafluorophenoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61436-52-0

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61436-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61436-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61436-52:
(7*6)+(6*1)+(5*4)+(4*3)+(3*6)+(2*5)+(1*2)=110
110 % 10 = 0
So 61436-52-0 is a valid CAS Registry Number.

61436-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name phenol,tetrafluoroniobium

1.2 Other means of identification

Product number -
Other names Niobium,tetrafluorophenoxy

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:61436-52-0 SDS

61436-52-0Downstream Products

61436-52-0Relevant academic research and scientific papers

Convenient synthesis of fluoride-alkoxides of Nb(v) and Ta(v): A spectroscopic, crystallographic and computational study

Bortoluzzi, Marco,Guazzelli, Nicola,Marchetti, Fabio,Pampaloni, Guido,Zacchini, Stefano

, p. 12898 - 12906 (2013/01/15)

The synthesis and the spectroscopic characterization of fluoride-alkoxides of niobium and tantalum in the highest oxidation state are reported. Suspensions of MF5 (M = Nb, Ta) in a chlorinated solvent reacted with up to three equivalents of ROSiMe3 (R = Me, Et, Ph) to afford polynuclear derivatives and variable amounts of FSiMe3. Thus MF4(OR) (R = Et, Ph) and MF3(OR)2 were obtained by selective 1:1 and 1:2 reactions almost exclusively as single isomeric products; otherwise mixtures of MF4(OMe) species were afforded from the equimolar reactions of MF5 with MeOSiMe3. The 1:3 reaction of TaF5 with MeOSiMe3 led to different forms of TaF 2(OMe)3. The synthesis of TaF(OPh)4 was forced by high temperature conditions or the use of a large excess of PhOSiMe 3. DFT studies were carried out in order to predict, in the distinct cases, the most stable structures of the metal products. The molecular structures of [NbF2(OPh)2(μ-F)]3 and [TaF(OPh)3(μ-OPh)]2 were ascertained by X-ray diffraction.

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