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Phosphorodiamidimidic chloride, N,N,N',N'-tetramethyl-N''-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19946-85-1

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19946-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19946-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,4 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19946-85:
(7*1)+(6*9)+(5*9)+(4*4)+(3*6)+(2*8)+(1*5)=161
161 % 10 = 1
So 19946-85-1 is a valid CAS Registry Number.

19946-85-1SDS

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 N-[chloro-(dimethylamino)-phenylimino-λ<sup>5</sup>-phosphanyl]-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names N,N,N',N'-tetramethyl-N''-phenylphosphorodiamidimidic chloride

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:19946-85-1 SDS

19946-85-1Relevant academic research and scientific papers

Guanidinophosphazenes: Design, synthesis, and basicity in THF and in the gas phase

Kolomeitsev, Alexander A.,Koppel, Ilmar A.,Rodima, Toomas,Barten, Jan,Lork, Enno,Roeschenthaler, Gerd-Volker,Kaljurand, Ivari,Kuett, Agnes,Koppel, Ivar,Maeemets, Vahur,Leito, Ivo

, p. 17656 - 17666 (2007/10/03)

A principle for creating a new generation of nonionic superbases is presented. It is based on attachment of tetraalkylguanidino, 1,3-dimethylimidazolidine-2-imino, or bis(tetraalkylguanidino)carbimino groups to the phosphorus atom of the iminophosphorane group using tetramethylguanidine or easily available 1,3-dimethylimidazolidine-2-imine. Seven new nonionic superbasic phosphazene bases, tetramethylguanidino-substituted at the P atom, have been synthesized. Their base strengths are established in tetrahydrofuran (THF) solution by means of spectrophotometric titration and compared with those of eight reference superbases designed specially for this study, P2- and P4-iminophosphoranes. The gas-phase basicities of several guanidino- and N′,N′,N″,N″-tetramethylguanidino (tmg)-substituted phosphazenes and their cyclic analogues are calculated, and the crystal structures of (tmg)3P=N-t-Bu and (tmg) 3P=N-t-Bu·HBF4 are determined. The enormous basicity-increasing effect of this principle is experimentally verified for the tetramethylguanidino groups in the THF medium: the basicity increase when moving from (dma)3P= N-t-Bu (pKα = 18.9) to (tmg) 3P=N-t-Bu (pKα = 29.1) is 10 orders of magnitude. A significantly larger basicity increase (up to 20 powers of 10) is expected (based on the high-level density functional theory calculations) to accompany the similar gas-phase transfer between the (dma)3P=NH and (tmg) 3P=NH bases. Far stronger basicities still are expected when, in the latter two compounds, all three dimethylamino (or tetramethylguanidino) fragments are replaced by methylated triguanide fragments, (tmg) 2C=N-. The gas-phase basicity (around 300-310 kcal/mol) of the resulting base, [(tmg)2C=N-]3P=NH, having only one phosphorus atom, is predicted to exceed the basicity of (dma)3P=NH by more than 40 powers of 10 and to surpass also the basicity of the widely used commercial [(dma)3P=N]3P=N-t-Bu (t-BuP4) superbase.

CATIONS PHOSPHORES A BASSE COORDINATION: LES IMINOPHOSPHENIUMS

Sanchez, M.,Marre, M. R.,Brazier, J. F.,Bellan, J.,Wolf, R.

, p. 331 - 334 (2007/10/02)

The novel iminophosphenium, 2P+=NC6H5, has been prepared by a modified Staudinger reaction.The mechanism of this process is discussed on the basis of spectroscopic studies of various derivatives of this ion.

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