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butyl bis(4-chlorophenyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42991-55-9

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42991-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42991-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,9 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42991-55:
(7*4)+(6*2)+(5*9)+(4*9)+(3*1)+(2*5)+(1*5)=139
139 % 10 = 9
So 42991-55-9 is a valid CAS Registry Number.

42991-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 2,2-bis(4-chlorophenyl)acetate

1.2 Other means of identification

Product number -
Other names Bis-(4-chlor-phenyl)-essigsaeure-butylester

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:42991-55-9 SDS

42991-55-9Downstream Products

42991-55-9Relevant academic research and scientific papers

Palladium/copper-catalyzed Di-α-arylation of acetic acid esters

Song, Bingrui,Himmler, Thomas,Goossen, Lukas J.

supporting information; experimental part, p. 1688 - 1694 (2011/09/14)

A bimetallic palladium/copper catalyst system was found to effectively promote the diarylation of alkyl acetates with aryl halides under unprecedentedly mild conditions. The phenanthroline-copper-phosphine catalyst stabilizes the enolate intermediate to the extent that the deprotonation of esters can be achieved even with the mild base potassium phosphate. The palladium tri-tert-butylphosphine co-catalyst mediates the coupling of the resulting copper enolate with a wide variety of aryl halides with selective formation of the corresponding diarylacetic acid esters. Copyright

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