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(4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol is a complex organic compound that features a piperazine ring, a methoxyphenyl group, and a phenylmethanol group. Classified as a piperazine derivative, (4-{3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxy}phenyl)methanol also contains a methoxy functional group. Its intricate molecular structure suggests potential applications in medicinal chemistry and research, where it could be utilized in the development of pharmaceutical drugs or serve as a chemical reagent. The presence of diverse functional groups endows (4-{3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxy}phenyl)methanol with a range of biological and pharmacological properties that warrant further investigation to fully understand its capabilities and effects.

119321-64-1

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119321-64-1 Usage

Uses

Used in Pharmaceutical Development:
(4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol is used as a chemical intermediate in the synthesis of various pharmaceutical drugs. Its unique structure, including the piperazine ring and methoxyphenyl group, allows it to interact with biological targets, potentially leading to the development of new medications with specific therapeutic effects.
Used in Medicinal Research:
In the field of medicinal research, (4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol serves as a valuable compound for studying the interactions between small molecules and biological systems. Its structural features may provide insights into the design of new drugs with improved efficacy and selectivity.
Used in Chemical Reagent Applications:
(4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol is used as a chemical reagent in various laboratory settings. Its functional groups can participate in a range of chemical reactions, making it a versatile tool for researchers working on the synthesis and modification of organic compounds.
Used in Drug Discovery:
In the drug discovery process, (4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol is used as a lead compound for the identification of potential therapeutic agents. Its structural elements may offer a starting point for the optimization of drug candidates, leading to the development of new treatments for various diseases and conditions.
Used in Chemical Synthesis Industry:
(4-3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxyphenyl)methanol is used as a key component in the synthesis of complex organic molecules. Its presence in the chemical synthesis industry highlights its importance in creating new compounds with diverse applications, from pharmaceuticals to materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 119321-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,2 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119321-64:
(8*1)+(7*1)+(6*9)+(5*3)+(4*2)+(3*1)+(2*6)+(1*4)=111
111 % 10 = 1
So 119321-64-1 is a valid CAS Registry Number.

119321-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[3-[4-(4-methoxyphenyl)piperazin-1-yl]propoxy]phenyl]methanol

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:119321-64-1 SDS

119321-64-1Downstream Products

119321-64-1Relevant academic research and scientific papers

Synthesis and Structure-Activity Relationship in 1-Aryloxy-3-1-(N4-arylpiperazinyl)>propanes

Agarwal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Sur, R. N.,Srimal, Rikhab C.,et al.

, p. 642 - 646 (2007/10/02)

1--3-1-(N4-arylpiperazinyl)>propanes (6, 7) have been synthesized by the condensation of 1-acetyl-1,2,3,4-tetrahydroquinoline with 1-chloro-3-1-(N4-arylpiperazinyl)>propane,

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