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9H-Fluorene, 1,2,3,4-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64465-03-8

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64465-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64465-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64465-03:
(7*6)+(6*4)+(5*4)+(4*6)+(3*5)+(2*0)+(1*3)=128
128 % 10 = 8
So 64465-03-8 is a valid CAS Registry Number.

64465-03-8SDS

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 1,2,3,4-tetraphenyl-9H-fluorene

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetraphenyl-fluoren

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:64465-03-8 SDS

64465-03-8Downstream Products

64465-03-8Relevant academic research and scientific papers

An unusual cobalt-mediated cleavage of a hindered alkyne

Hayashi, Naoto,Ho, Douglas M.,Pascal Jr., Robert A.

, p. 4261 - 4264 (2000)

When 1-(pentaphenylphenyl)-2-phenylacetylene (1) is heated with (η5- cyclopentadienyl)dicarbonylcobalt, 1,2,3,4-tetraphenylfluorene (3) and related minor products are formed rather than the expected tetraarylcyclobutadiene. The formation of 3 requires that a seven-carbon fragment (formally a phenylcarbyne) must be lost. Two minor products, however, result from intramolecular cyclization of the alkyne and these two retain all of the carbons from the starting material. (C) 2000 Elsevier Science Ltd.

Coupling of the R-Cp or indenyl ligand with the diene moiety of bis(substituted cyclopentadienyl)- or bis(indenyl)zirconacyclopentadienes

Ren, Shenyong,Igarashi, Eri,Nakajima, Kiyohiko,Kanno, Ken-ichiro,Takahashi, Tamotsu

supporting information; experimental part, p. 7492 - 7493 (2009/10/17)

(Chemical Equation Presented) When bis(substituted cyclopentadienyl)- orbis(indenyl)zirconacyclopentadienes were treated with TiCl4, a coupling reaction between the substituted cyclopentadienyl or indenyl ligand and the diene moiety proceeded to give indene or fluorene deriva tives in moderate to high yields. With the sterically hindered t-Bu-substituted Cp ligand, the coupling products were obtained in high yields.

Polycyclic Aromatic Compounds : Part I - A New Synthesis of Fluorenone Fluorene Derivatives

Bandyopadhyay, T. K.,Bhattacharya, A. J.

, p. 439 - 442 (2007/10/02)

A series of hitherto unknown highly substituted fluorenone and fluorene derivatives has been synthesised.The synthesis involves Diels-Alder cycloaddition reaction of cyclopentadienones with ethyl esters of phenyl- and p-methylphenylpropiolic acids.The add

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