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CYCLOBUTYL 4-TRIFLUOROMETHYLPHENYL KETONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53342-40-8

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53342-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53342-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53342-40:
(7*5)+(6*3)+(5*3)+(4*4)+(3*2)+(2*4)+(1*0)=98
98 % 10 = 8
So 53342-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H11F3O/c13-12(14,15)10-6-4-9(5-7-10)11(16)8-2-1-3-8/h4-8H,1-3H2

53342-40-8SDS

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 cyclobutyl-[4-(trifluoromethyl)phenyl]methanone

1.2 Other means of identification

Product number -
Other names CYCLOBUTYL 4-TRIFLUOROMETHYLPHENYL KETONE

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:53342-40-8 SDS

53342-40-8Upstream product

53342-40-8Downstream Products

53342-40-8Relevant academic research and scientific papers

Cobalt-catalyzed acylation-reactions of (hetero)arylzinc pivalates with thiopyridyl ester derivatives

Lutter, Ferdinand H.,Grokenberger, Lucie,Hofmayer, Maximilian S.,Knochel, Paul

, p. 8241 - 8245 (2019)

A cobalt-catalyzed acylation reaction of various primary, secondary and tertiary alkyl, benzyl and (hetero)aryl S-pyridyl thioesters with (hetero)arylzinc pivalates is reported. The thioesters were prepared directly from the corresponding carboxylic acids under mild conditions, thus tolerating sensitive functional groups. Acylations of α-chiral S-pyridyl esters proceeded with very high stereoretention leading to optically enriched α-chiral ketones.

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