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55975-53-6

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55975-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55975-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,7 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55975-53:
(7*5)+(6*5)+(5*9)+(4*7)+(3*5)+(2*5)+(1*3)=166
166 % 10 = 6
So 55975-53-6 is a valid CAS Registry Number.

55975-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-2,4,4,6,6-pentakis-(2,2,2-trifluoro-ethoxy)-2λ5,4λ5,6λ5-cyclotriphosphazene

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:55975-53-6 SDS

55975-53-6Downstream Products

55975-53-6Relevant articles and documents

Effects of Mass Transfer and Extraction of Quarternary Salts on a Substitution Reaction by Phase-Transfer Catalysis

Wang, Maw-Ling,Wu, Ho-Sheng

, p. 2344 - 2350 (2007/10/02)

The substitution reaction of hexachlorocyclotriphosphazene with 2,2,2-trifluoroethanol using quaternary ammonium salts as the phase-transfer catalysts in an organic solvent/alkaline solution has been investigated.The pseudo-first-order reaction rate constant of the two-phase reaction and the rate constant ratios of the sequential substitution reaction in the organic phase were obtained.The hydration number of the catalyst, QOCH2CF3, is determined from the experimental data.The reaction reactivity is influenced by the content of the acids, which include water and alcohol in the aqueous phase.For an extraction mechanism, the reactivities of all kinds of catalysts in the organic phase with the same kind of solvent are the same.The effects of mass transfer and the extraction of quaternary ammonium salts on the conversion are used to explain the experimental data.The obtained results can be used as a reference for selecting the appropriate solvent and catalyst as well as for determining the appropriate content in the aqueous phase.Meanwhile, the desired distributed products, including the intermediate and final products, can be obtained by the appropriate choice of reaction conditions.

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