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(2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one is a complex organic compound featuring a fluorophenyl group, a piperazine ring, and a trifluoromethylphenyl group. As an enone, it has a carbon-carbon double bond conjugated to a carbonyl group, which may contribute to its chemical reactivity and potential applications. The presence of the piperazine ring, a common structural element in drug design due to its biological activity, suggests that (2Z)-1-(3-fluorophenyl)-3-{4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}but-2-en-1-one could have pharmaceutical relevance. The combination of these functional groups and the conjugated double bond make this molecule a promising candidate for further exploration in medicinal chemistry and organic synthesis.

76691-09-3

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76691-09-3 Usage

Uses

Used in Pharmaceutical Industry:
(2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one is used as a potential pharmaceutical agent for its possible biological activity, stemming from the presence of the piperazine ring and the compound's overall structure. The specific application reason would depend on the results of further research into its pharmacological properties and potential therapeutic effects.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one serves as a subject for study to understand its interactions with biological targets and its potential as a lead compound in drug development. (2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one's unique structure, including the fluorophenyl and trifluoromethylphenyl groups, may offer insights into structure-activity relationships and the design of new therapeutic agents.
Used in Organic Synthesis:
(2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one is utilized as a starting material or intermediate in organic synthesis for the development of new compounds with potential applications in various fields, including materials science, agrochemicals, and specialty chemicals. (2Z)-1-(3-fluorophenyl)-3-4-[3-(trifluoromethyl)phenyl]piperazin-1-ylbut-2-en-1-one's reactivity and functional group diversity make it a valuable component in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 76691-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76691-09:
(7*7)+(6*6)+(5*6)+(4*9)+(3*1)+(2*0)+(1*9)=163
163 % 10 = 3
So 76691-09-3 is a valid CAS Registry Number.

76691-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-fluorophenyl)-3-[4-[3-(trifluoromethyl)phenyl]piperazin-1-yl]but-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:76691-09-3 SDS

76691-09-3Downstream Products

76691-09-3Relevant academic research and scientific papers

N-Substituted 2- & 3-Alkyl-3-aminoacrylopheones & Some Related Compounds as Antiinflammatory Agents

Pratap, Ram,Gupta, R. C.,Srimal, R. C.,Anand, Nitya

, p. 695 - 698 (2007/10/02)

Synthesis and biological evaluation of some 2- and 3-alkyl-3-aminoacrylophenones and 2-methylcinnamides are reported.The stereochemistry of the products has been assigned on the basis of PMR spectra using Eu(fod)3 shift reagent.Some of these compounds hav

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