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13596-41-3

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13596-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13596-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13596-41:
(7*1)+(6*3)+(5*5)+(4*9)+(3*6)+(2*4)+(1*1)=113
113 % 10 = 3
So 13596-41-3 is a valid CAS Registry Number.

13596-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pentakisphosphorus nitride dichloride

1.2 Other means of identification

Product number -
Other names phosphonitrile dichloride cyclic pentamer

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:13596-41-3 SDS

13596-41-3Relevant articles and documents

Structure and conformation of the medium-sized chlorophosphazene rings

Bowers, David J.,Wright, Brian D.,Scionti, Vincenzo,Schultz, Anthony,Panzner, Matthew J.,Twum, Eric B.,Li, Lin-Lin,Katzenmeyer, Bryan C.,Thome, Benjamin S.,Rinaldi, Peter L.,Wesdemiotis, Chrys,Youngs, Wiley J.,Tessier, Claire A.

, p. 8874 - 8886 (2014/12/09)

Medium-sized cyclic oligomeric phosphazenes [PCl2N]m (where m = 5-9) that were prepared from the reaction of PCl5 and NH4Cl in refluxing chlorobenzene have been isolated by a combination of sublimation/extraction and column chromatography from the predominant products [PCl2N]3 and [PCl2N]4. The medium-sized rings [PCl2N]m have been characterized by electrospray ionization-mass spectroscopy (ESI-MS), their 31P chemical shifts have been reassigned, and their T1 relaxation times have been obtained. Crystallographic data has been recollected for [PCl 2N]5, and the crystal structures of [PCl 2N]6, and [PCl2N]8 are reported. Halogen-bonding interactions were observed in all the crystal structures of cyclic [PCl2N]m (m = 3-5, 6, 8). The crystal structures of [P(OPh)2N]7 and [P(OPh)2N]8, which are derivatives of the respective [PCl2N]m, are also reported. Comparisons of the intermolecular forces and torsion angles of [PCl2N]8 and [P(OPh)2N]8 with those of three other octameric rings are described. The comparisons show that chlorophosphazenes should not be considered prototypical, in terms of solid-state structure, because of the strong influence of halogen bonding.

A new route to the phosphazene polymerization precursors, Cl3P=NSiMe3 and (NPCl2)3

Allcock, Harry R.,Crane, Chester A.,Morrissey, Christopher T.,Olshavsky, Michael A.

, p. 280 - 283 (2008/10/08)

An improved synthesis of the phosphazene polymerization precursors, hexachlorocyclotriphosphazene, (NPCl2)3 (1), and Cl3P=NSiMe3 (2) is reported. The addition of PCl5 to N(SiMe3)3 in methylene chloride at 40 °C produced a mixture of phosphazenes which contained 76% of 1. However, the addition of N(SiMe3)3 to PCl5 in methylene chloride at 0 °C, followed by the addition of hexane, provided 2 in 40% yield. The mechanism of the reaction is discussed.

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