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Piperazine, 1-(2-phenylethyl)-4-(2-pyridinyl)-, is a chemical compound belonging to the piperazine class of organic molecules. It features a piperazine ring with a phenylethyl group and a pyridinyl group attached, offering potential therapeutic properties that make it valuable in pharmaceutical research and drug development.

1033-69-8

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1033-69-8 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Piperazine, 1-(2-phenylethyl)-4-(2-pyridinyl)is utilized as a compound with potential therapeutic properties for the treatment of various medical conditions. Its unique structure allows it to be a candidate for addressing psychiatric disorders and neurological diseases due to its interaction with specific biological targets.
Used in the Synthesis of Complex Organic Compounds:
In the chemical industry, Piperazine, 1-(2-phenylethyl)-4-(2-pyridinyl)serves as a building block for the synthesis of more complex organic compounds. Its versatile structure enables the creation of a wide range of molecules with diverse applications in various fields, including medicinal chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1033-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1033-69:
(6*1)+(5*0)+(4*3)+(3*3)+(2*6)+(1*9)=48
48 % 10 = 8
So 1033-69-8 is a valid CAS Registry Number.

1033-69-8SDS

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-(2-Phenylethyl)-4-(2-pyridinyl)piperazine

1.2 Other means of identification

Product number -
Other names 1-phenethyl-4-pyridin-2-yl-piperazine

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:1033-69-8 SDS

1033-69-8Downstream Products

1033-69-8Relevant academic research and scientific papers

N-nrylalkylpiperidines as high-affinity sigma-1 and sigma-2 receptor ligands: Phenylpropylamines as potential leads for selective sigma-2 agents

Maeda, Dean Y.,Williams, Wanda,Kim, Wes E.,Thatcher, Linn N.,Bowen, Wayne D.,Coop, Andrew

, p. 497 - 500 (2007/10/03)

To delineate the differences between the structural requirements necessary for recognition at sigma-1 and sigma-2 receptors, a range of phenethyl- and phenylpropylpiperidines were evaluated in binding assays. Phenethylpiperidines were found to favor sigma-1 receptors, whereas phenylpropylpiperidines tend to favor sigma-2 receptors. It appears that phenylpropylamine is a potential pharmacophore for selective sigma-2 ligands.

New μ-opioid receptor agonists with piperazine moiety

Komoto,Okada,Sato,Niino,Oka,Sakamoto

, p. 1314 - 1320 (2007/10/03)

New μ-opioid receptor (MOR) agonists containing piperazine and homopiperazine moieties in the structures were synthesized and their affinities to and agonist potencies on MOR were evaluated. Among the synthesized compounds, 4-[4-(2-methoxyphenyl)piperazin-1-yl]-N,N-dimethyl-2,2-diphenylbutanamide (20Aa) showed the highest affinity to the human MOR expressed in Chinese hamster ovary (CHO)-K1 cells, and the highest agonist potency on the MOR in isolated guinea-pig ileum preparation.

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