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Pyrimidine, 4,6-bis[5'-[(hexadecyloxy)methyl][2,2'-bipyridin]-6-yl]-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

877455-80-6

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877455-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877455-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,4,5 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 877455-80:
(8*8)+(7*7)+(6*7)+(5*4)+(4*5)+(3*5)+(2*8)+(1*0)=226
226 % 10 = 6
So 877455-80-6 is a valid CAS Registry Number.

877455-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-bis{6'-[5''-(hexadecyloxymethyl)pyrid-2''-yl]pyrid-2'-yl}-2-phenylpyrimidine

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:877455-80-6 SDS

877455-80-6Upstream product

877455-80-6Downstream Products

877455-80-6Relevant academic research and scientific papers

Two morphologies of stable, highly ordered assemblies of a long-chain-substituted [2 × 2]-grid-type FeII complex adsorbed on HOPG

Mourran, Ahmed,Ziener, Ulrich,Moeller, Martin,Breuning, Esther,Ohkita, Masakazu,Lehn, Jean-Marie

, p. 2641 - 2647 (2005)

The programmed self-assembly of a multimetallic grid-type supramolecular architecture and its hierarchical organization on graphite are described. The doubly functionalized 4,6-bis(2,2′-bipyridyl-6-yl)-2-phenylpyrimidine derivative 1, equipped with CH2OC16H33 moieties at the terminal pyridine rings, was designed as a new bis(tridentate) ligand and synthesized using Stille-type coupling reactions. Treatment of ligand 1 with Fe(BF4)2·6H2O in CHCl 3/CH3CN led to the spontaneous formation of a [2 × 2]-grid-type FeII complex 2 in quantitative yield. The self-assembled tetranuclear complex 2 was adsorbed onto highly oriented pyrolytic graphite (HOPG) and studied by scanning tunneling microscopy (STM), which showed two morphologies of highly ordered two-dimensional arrays of the metallo-supramolecular archi tectures. The resulting monolayers of the grid-type complex 2 are much more stable than that obtained from the corresponding unsubstituted grid-type complex owing to the additional attractive forces between the hexadecyl moieties in 2 and the HOPG surface. Moreover, the reproducibility of the STM images of the hexadecyl-substituted grid 2 was strongly improved compared to the unsubstituted one. These results suggest that the introduction of long alkyl chains into metallo-supramolecular architectures would have general advantages for their organization and STM investigation on HOPG. Details of the preparation and the STM investigation of ligand 1 are also presented. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

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