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Phosphine oxide, [1,3,5-benzenetriyltris(methylene)]tris[diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73218-92-5

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73218-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73218-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,1 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73218-92:
(7*7)+(6*3)+(5*2)+(4*1)+(3*8)+(2*9)+(1*2)=125
125 % 10 = 5
So 73218-92-5 is a valid CAS Registry Number.

73218-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-tris(diphenylphosphorylmethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,3,5-tris(diphenylphosphorymethyl)benzene

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:73218-92-5 SDS

73218-92-5Relevant academic research and scientific papers

Trifunctional phosphane ligands and their application in the synthesis of novel cage-structured platinacyclophanes and trinuclear chain-like platinacycles by self-assembly

Lindner, Ekkehard,Khanfar, Monther,Steimann, Manfred

, p. 2411 - 2419 (2007/10/03)

The synthesis of the 1,3,5-tris[(diphenylphosphoryl)alkyl]-benzenes 7-10 succeeds by reaction of the corresponding 1,3,5-tris(bromoalkyl)benzenes 3-6 with ethyl diphenylphosphinite in an Arbusov-type reaction. Reduction of these phosphane oxides leads to the trifunctional phosphane ligands 11-14. Their potency of self-assembly was examined by the employment of platinum(II) complex fragments. A five-component self-assembly consisting of 3 equiv, of the platinum complex Cl2Pt(NCPh)2 and 2 equiv, of the ligands 11-14 under high-dilution conditions led to the formation of the nanoscaled triplatinacyclophanes 1 and 15-17. Polymers were formed as by-products from the reactions between 11-13 and Cl2Pt(NCPh)2, whereas in the case of 14 three other platinacyles 18-20 with a chain-like structure were formed. The structures of the metallacycles 1 and 15-17 as well as 18-20 were elucidated by 31p{1H}, 13C{1H}, and 195Pt{1H} NMR spectroscopic investigations.

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