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Methanone, (4-chlorophenyl)(pentachlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60921-35-9

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60921-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60921-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,2 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60921-35:
(7*6)+(6*0)+(5*9)+(4*2)+(3*1)+(2*3)+(1*5)=109
109 % 10 = 9
So 60921-35-9 is a valid CAS Registry Number.

60921-35-9SDS

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-chlorophenyl)-(2,3,4,5,6-pentachlorophenyl)methanone

1.2 Other means of identification

Product number -
Other names p-Chlorphenyl-pentachlorphenyl-keton

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:60921-35-9 SDS

60921-35-9Upstream product

60921-35-9Downstream Products

60921-35-9Relevant academic research and scientific papers

Aryl(pentachlorophenyl)nickel(II) complexes. Lack of free rotation about tolyl-nickel bonds and lack of ortho effect in carbonylation

Wada, Masanori,Kusabe, Koji,Oguro, Keisuke

, p. 446 - 449 (2007/10/13)

A series of complexes of the type trans-R(C6Cl5)Ni(PPhMe2)2 (where R = aryl) was prepared. Their 1H NMR spectra indicate that both R = o-tolyl and m-tolyl groups are oriented perpendicularly to the nickel coordination plane. Reaction of carbon monoxide with these complexes gave, under mild conditions, R(C6Cl5)CO for R = aryl groups including o-tolyl but not for 2-furyl and its analogues. The o-tolyl complex was exceptionally stable toward thermal reductive elimination in tetrachloroethylene under air. Factors affecting the relative reactivities of these complexes are discussed, based mainly on the early explanation for the so-called ortho effect .

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