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Anilinotriphenylphosphonium bromide is a complex organic compound with the chemical formula C18H15BrNP. It is a derivative of triphenylphosphine, where one of the phenyl groups is replaced by an aniline group. anilinotriphenylphosphonium bromide is a colorless crystalline solid, soluble in organic solvents, and is often used as a phase-transfer catalyst in organic synthesis. It facilitates the transfer of reactants between aqueous and organic phases, thereby enhancing the efficiency of various chemical reactions. Anilinotriphenylphosphonium bromide is also known for its ability to form stable complexes with metal ions, making it a useful reagent in coordination chemistry. Its unique structure and properties have led to its application in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.

6395-93-3

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6395-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6395-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6395-93:
(6*6)+(5*3)+(4*9)+(3*5)+(2*9)+(1*3)=123
123 % 10 = 3
So 6395-93-3 is a valid CAS Registry Number.

6395-93-3SDS

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 anilinotriphenylphosphomium bromide

1.2 Other means of identification

Product number -
Other names Bromid

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:6395-93-3 SDS

6395-93-3Relevant academic research and scientific papers

Complexes of N-aryltriphenylphosphinimines with mercury(II) halides

Braun, Thomas P.,Gutsch, Paul A.,Zimmer, Hans

, p. 858 - 862 (2007/10/03)

The synthesis IR and 31P NMR spectra of the complexes of various N-aryltriphenylphosphinimines with some mercury dihalides as well as the corresponding phosphonium salts are reported It is shown by an X-ray crystal structure analysis of the complex of the unsubstituted phosphinimine with HgCl2 that in the solid state these complexes form dimers via two Hg...μ2 Cl...Hg bridges.

THE SYNTHESIS AND CHARACTERIZATION OF MIXED (ALKYLAMINO) AND (ARYLAMINO)PHENYLPHOSPHONIUM COMPOUNDS

Fuente, German F. de la,Huheey, James E.

, p. 23 - 36 (2007/10/02)

The syntheses of alkyl and aryl-substituted tetrakis(amino)phenylphosphonium compounds of type (RNH)4-n(C6H5)nPX, where R = n-C3H7 (1), i-C3H7 (2), n-C4H9 (3), s-C4H9 (4), n-C6H13 (5), c-C6H11 (6), C6H5CH2 (7) and C6H5 (8), and where

SYNTHESIS AND CH-ACIDITY OF N,N-DISUBSTITUTED AMINOTRIPHENYLPHOSPHONIUM SALTS

Kabachnik, M. I.,Lobanov, D. I.,Matveeva, A. G.,Kovsheva, O. E.,Terekhova, M. I.,et al.

, p. 1417 - 1422 (2007/10/02)

Several substituted methylaminotriphenylphosphonium salts (APS) of general formula +N(R)CH2R'>X- have been synthesized.The CH-acidities of some of the prepared APS have been measured by the indicator method in DMSO, with K+ counterion and 9-phenylfluorene (pK 18.5) as standard, showing a pK range of 14.7-24.8.The acidification effect of Ph3P+N(Ph) (?CH2- = 0.70) and Ph3P+N(Bu) (?CH2- = 0.68) groups has been evaluated.The results obtained suggest that there is an effective charge on the nitrogen atom in the APS studied and an increased multiplicity of the N-P bond.

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