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1-Octanone, 1-(4-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111829-15-3

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111829-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111829-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,2 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111829-15:
(8*1)+(7*1)+(6*1)+(5*8)+(4*2)+(3*9)+(2*1)+(1*5)=103
103 % 10 = 3
So 111829-15-3 is a valid CAS Registry Number.

111829-15-3SDS

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 1-(4-fluorophenyl)octan-1-one

1.2 Other means of identification

Product number -
Other names 1-Octanone,1-(4-fluorophenyl)

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:111829-15-3 SDS

111829-15-3Downstream Products

111829-15-3Relevant academic research and scientific papers

Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids

Roslin, Sara,Odell, Luke R.

supporting information, p. 6895 - 6898 (2017/07/10)

Herein, a simple and efficient method for the palladium-catalyzed carbonylation of aryl boronic acids with unactivated alkyl iodides and bromides under visible-light irradiation, ambient temperature and low CO-pressure is presented. Notably, the procedure uses readily available equipment and an inexpensive palladium catalyst to generate the key alkyl radical intermediate. These mild conditions enabled the synthesis of a range of functionalized aryl alkyl ketones including the antipsychotic drug, melperone.

α-Arylation, α-arylative esterification, or acylation: A stoichiometry-dependent trichotomy in the Pd-catalyzed cross-coupling between aldehydes and aryl bromides

Nareddy, Pradeep,Mazet, Clement

supporting information, p. 2579 - 2583 (2013/11/19)

Three′s company: The selective α-arylation and α-arylative esterification of linear and branched aldehydes is reported for a variety of bromoarenes. The acylation of aryl bromides can be achieved with linear aldehydes (see scheme). All these transformations were performed with a single [(N-heterocyclic carbene)Pd] catalyst through adjustment of the stoichiometry of the reagents and the appropriate base. Copyright

Synthesis of aryl fluorides on a solid support and in solution by utilizing a fluorinated solvent

Doebele, Marion,Vanderheiden, Sylvia,Jung, Nicole,Braese, Stefan

supporting information; experimental part, p. 5986 - 5988 (2010/10/01)

(Figure Presented) F for fast: The perfluorinated solvent C 6F14 is the key to a new variant of the BalzSchiemann reaction for the synthesis of fluorinated arenes. Triazenes are converted into fluoroarenes under mild con-ditions on a support and in solution (see scheme). The method is straightforward and inexpensive, and yields previously difficult-to-prepare fluoroarenes in high purity.

Iron catalyst for oxidation in water: Surfactant-type iron complex-catalyzed mild and efficient oxidation of aryl alkanes using aqueous TBHP as oxidant in water

Nagano, Takashi,Kobayashi, Shu

supporting information; experimental part, p. 1042 - 1043 (2009/12/02)

Surfactant-type iron(III) complex, Fe2O(DS)4, was found to be effective for benzylic oxidation of simple aryl alkanes using aqueous t-butyl hydroperoxide (TBHP) as an oxidant. Copyright

Highly efficient chromium-catalyzed oxidation of secondary benzylic alcohols by aqueous 70% tert-butyl hydroperoxide

Muzart,N'Ait Ajjou

, p. 785 - 787 (2007/10/02)

The oxidation of secondary benzylic alcohols to ketones by the chromium(VI) oxide/tert-butyl hydroperoxide system is compatible with the presence of methyl, halide, methoxy, acetoxy or nitro substituents on the aryl group and of an unsaturation on the alkyl side chain. Benzyl alcohol led to a mixture of benzaldehyde and benzoic acid.

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