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1-(3,5-Dimethylphenyl)piperazine is a chemical compound that belongs to the class of organic compounds known as diarylethers. Diarylethers are characterized by the presence of two aryl groups connected by an ether group. This specific compound is notable for its solid powder form, featuring a benzene ring with adjacent methyl groups and a piperazine substitute. These structural features confer upon it properties that are advantageous for various chemical reactions, although its specific applications in industrial, medical, or commercial settings are not extensively detailed in the literature, indicating a need for further exploration and research.

105907-65-1

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105907-65-1 Usage

Uses

Given the lack of explicit applications detailed in the provided materials, the uses of 1-(3,5-Dimethylphenyl)piperazine can only be inferred based on its chemical class and structural properties. Here are some potential uses based on its classification as a diarylether and the general properties of similar compounds:
Used in Chemical Synthesis:
1-(3,5-Dimethylphenyl)piperazine is used as a building block or intermediate in the synthesis of more complex organic molecules for various applications, including pharmaceuticals, agrochemicals, and materials science, due to its reactive aryl and ether groups.
Used in Pharmaceutical Development:
As a component of diarylether compounds, 1-(3,5-Dimethylphenyl)piperazine may be used as a precursor or modifier in the development of pharmaceutical agents, potentially influencing the compound's biological activity and selectivity.
Used in Material Science:
1-(3,5-Dimethylphenyl)piperazine's structural features could make it suitable for use in the development of new materials with specific properties, such as in polymers or as part of sensor technologies, given the potential for interaction with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 105907-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105907-65:
(8*1)+(7*0)+(6*5)+(5*9)+(4*0)+(3*7)+(2*6)+(1*5)=121
121 % 10 = 1
So 105907-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2/c1-10-7-11(2)9-12(8-10)14-5-3-13-4-6-14/h7-9,13H,3-6H2,1-2H3

105907-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-Dimethylphenyl)piperazine

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105907-65-1 SDS

105907-65-1Relevant academic research and scientific papers

Practical method for parallel synthesis of diversely substituted 1-phenylpiperazines

Konstantinova, Igor,Bukhryakov, Konstantin,Gezentsvey, Yuri,Krasavin, Mikhail

experimental part, p. 628 - 630 (2012/05/21)

A simple and practical method to prepare 'libraries' of substituted 1-phenylpiperazine building blocks in parallel format has been developed.

Urea derivative useful as an anti-cancer agent and process for preparing same

-

, (2008/06/13)

The present invention relates to a novel urea derivative represented by the following formula (I), which is useful as an anti-cancer agent: 1its pharmaceutically acceptable acid addition salt or stereoisomer, in which X, Y, B and Het have the meaning as

SYNTHESE DE N,N-DIALKYL-3,5-DIALKYL-ANILINES A PARTIR DES SELS DE TRIALKYL-2,4,6-PYRYLIUM

Vernaudon, Pascal,Rajoharison, Harivelo G.,Roussel, Chritian

, p. 205 - 211 (2007/10/02)

We have optimized through an experimental design the synthesis of N,N-diethyl-3,5-dimethylaniline from 2,4,6-trimethylpyrylium terafluoroborate (I) and diethylamine in a new reaction medium (acetonitrile/triethylamine).Optimal conditions have been applied with high yields to the synthesis of various 3,5-dimethylanilines derived from I and dimethylamine, morpholine, N-methylpiperazine, piperazine, dihexylamine, piperidine, and pyrrolidine respectively. 2-Alkyl-4,6-dimethylpyrylium tetrafluoroborates react regioselectively with diethylamine to afford N,N-diethyl-3-alkyl-5-methyl anilines under these conditions.

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