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4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline is a complex organic compound with the molecular formula C12H17F3N2O and a molecular weight of 266.27 grams per mole. It features a heterocyclic amine, the piperazine ring, linked to a trifluoromethylated aniline group, and an acetyl group, indicating its potential as an acetylating agent. As a research chemical, its properties such as melting point, boiling point, and solubility in various solvents may vary and are typically specified by suppliers. Primarily used for research purposes, it is not commonly found in commercial or household products.

914348-88-2

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914348-88-2 Usage

Uses

Used in Research Applications:
4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline is used as a research chemical for [application reason] in the field of [specific research area or industry]. Its unique structure and functional groups make it a valuable compound for studying [specific research topic or purpose].
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline is used as a starting material or intermediate in the synthesis of potential drug candidates. Its acetylating properties and the presence of the trifluoromethyl group may contribute to the development of new therapeutic agents with improved pharmacological properties.
Used in Chemical Synthesis:
4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline is used as a building block in the synthesis of various complex organic molecules. Its versatile structure allows for further functionalization and modification, making it a valuable component in the creation of novel compounds with specific applications in different industries.
Used in Material Science:
In the field of material science, 4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline may be used as a component in the development of new materials with unique properties. Its incorporation into polymers or other materials could lead to the creation of materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 914348-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 914348-88:
(8*9)+(7*1)+(6*4)+(5*3)+(4*4)+(3*8)+(2*8)+(1*8)=182
182 % 10 = 2
So 914348-88-2 is a valid CAS Registry Number.

914348-88-2SDS

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 1-[4-[4-amino-2-(trifluoromethyl)phenyl]piperazin-1-yl]ethanone

1.2 Other means of identification

Product number -
Other names 4-(4-Acetyl-piperazin-1-yl)-2-trifluoromethylaniline

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:914348-88-2 SDS

914348-88-2Downstream Products

914348-88-2Relevant academic research and scientific papers

Nitrogen-containing heterocyclic compound and medicinal composition and application thereof

-

, (2021/05/29)

The invention provides a nitrogen-containing heterocyclic compound with a structure represented by a formula I, or a pharmaceutically acceptable salt, a stereoisomer or a prodrug molecule thereof, and a pharmaceutical composition and application thereof. The compound and the pharmaceutically acceptable salt thereof have an inhibition effect on RIOK2 protease, can effectively inhibit the growth of various tumor cells, and can be used for preparing antitumor drugs.

Design, synthesis and SAR study of 2-aminopyrimidines with diverse Michael addition acceptors for chemically tuning the potency against EGFRL858R/T790M

Chen, Wenteng,Liu, Shuangrong,Liu, Xingyu,Pan, Youlu,Shao, Jiaan

, (2020/08/10)

The covalent binding nature of irreversible kinase inhibitors potentially increases the severity of “off-target” toxicity. Based on our continual strategy of chemically tuning the Michael addition acceptors, herein, we further explore the relationship amo

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