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Phosphonium, (2-aminophenyl)triphenyl-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140669-73-4

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140669-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140669-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140669-73:
(8*1)+(7*4)+(6*0)+(5*6)+(4*6)+(3*9)+(2*7)+(1*3)=134
134 % 10 = 4
So 140669-73-4 is a valid CAS Registry Number.

140669-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-aminophenyl)triphenylphosphonium bromide

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:140669-73-4 SDS

140669-73-4Relevant academic research and scientific papers

Preparation of Hybrid Bidentate Phosphine Ligands by Reduction of Their Benzyl- or Phenyl-phosphonium Salts. X-Ray Crystal Structure of 2-Aminophenyltriphenylphosphonium Tetrachloronickelate(II)

Cooper, Mervyn K.,Downes, J. Michael,Duckworth, Paul A.,Tiekink, Edward R. T.

, p. 595 - 609 (2007/10/02)

The 2-substituted phenylphosphine bidentate hybrid ligands, 2-aminophenyl-, 2-methylaminophenyl-, 2-hydroxyphenyl- and (2-amino-3-methylphenyl)-diphenylphosphine, (1a-d), respectively, and 2-aminophenylmethylphenylphosphine, (1e), were synthesized by reduction of their phenylphosphonium halides, (2a-e)X (X = Cl or Br), with sodium naphthalenide in tetrahydrofuran at -68 deg, or electrochemically at a mercury cathode.The phosphonium salts were prepared by reaction of triphenylphosphine with aryl halide and anhydrous nickel halide at 200 deg.X-Ray diffraction of (2a)2 showed it to have monoclinic space group P21/n, a 10.657(4), b 20.966(3), c 20.422(6) Angstroem, β 101.33(2) deg and Z 4.The structure was refined by a full-matrix least-squares procedure to a final R 0.050 for 3534 reflections with I > 2.5?(I).

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