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3-(pentafluorophenyl)-1-phenylprop-2-en-1-one is a synthetic organic compound characterized by its unique molecular structure. It features a pentafluorophenyl group, which consists of a benzene ring with five fluorine atoms, attached to a prop-2-en-1-one backbone. This backbone is a three-carbon chain with a carbonyl group (C=O) at one end and a double bond between the second and third carbon atoms. The phenyl group, another benzene ring, is attached to the first carbon of the prop-2-en-1-one chain. 3-(pentafluorophenyl)-1-phenylprop-2-en-1-one is known for its potential applications in various chemical and pharmaceutical industries, particularly as an intermediate in the synthesis of more complex molecules. Its stability and reactivity can be influenced by the electron-withdrawing nature of the fluorine atoms, which can affect its chemical properties and make it a subject of interest in fluorine chemistry.

54081-32-2

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54081-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54081-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,8 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54081-32:
(7*5)+(6*4)+(5*0)+(4*8)+(3*1)+(2*3)+(1*2)=102
102 % 10 = 2
So 54081-32-2 is a valid CAS Registry Number.

54081-32-2SDS

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 (2E)-3-(Pentafluorophenyl)-1-phenyl-2-propen-1-one

1.2 Other means of identification

Product number -
Other names 2,3,4,5,6-Pentafluorchalcon

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:54081-32-2 SDS

54081-32-2Relevant academic research and scientific papers

Reactions of polyfluorinated chalcones with o-aminobenzenethiol and its zinc salt

Shmuilovich,Orlova,Beregovaya,Shelkovnikov

experimental part, p. 361 - 367 (2011/11/05)

The reactions of polyfluorochalcones with o-aminothiophenol in methanol in the presence of HCl afford polyfluorine-substituted 2,3-dihydrobenzo[b][1,5] thiazepines. In some cases, the cyclization is accompanied by fluorine substitution in the perfluorophenyl ring. Probably, the formation of thiazepines proceeds through the Michael thia-adduct. The Zn salt of o-aminothiophenol reacts with chalcones in DMF exclusively via fluorine substitution.

Ein neuer Zugang zu substituierten 5,6,7,8-Tetrafluorchinolinen

Bader, H.J.,Schuetz, G.,Wenck, H.

, p. 457 - 460 (2007/10/02)

The reaction of 2,3,4,5,6-pentafluorochalkones in ammonium acetate/glacial acetic acid yields 5,6,7,8-tetrafluoroquinolines.In addition 4-pentafluorophenyl-2,6-diphenylpyridines are formed.

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