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α-[(2-Fluorophenoxy)methyl]-4-phenyl-1-piperazineethanol is a complex organic compound with the molecular formula C20H22FNO2. It is a derivative of piperazine, a heterocyclic amine, and features a fluorophenoxy group attached to the piperazine ring. α-[(2-Fluorophenoxy)methyl]-4-phenyl-1-piperazineethanol is known for its potential applications in the pharmaceutical industry, particularly as a serotonin receptor agonist. It is structurally related to drugs that target the serotonin system, which plays a crucial role in mood regulation, appetite, and other physiological processes. The presence of the fluorine atom in the phenoxy group may confer specific pharmacological properties, such as altered metabolic stability or receptor binding affinity, compared to non-fluorinated analogs. The compound's structure and potential therapeutic uses make it an interesting subject for further research in medicinal chemistry.

66307-47-9

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66307-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66307-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66307-47:
(7*6)+(6*6)+(5*3)+(4*0)+(3*7)+(2*4)+(1*7)=129
129 % 10 = 9
So 66307-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H23FN2O2/c20-18-8-4-5-9-19(18)24-15-17(23)14-21-10-12-22(13-11-21)16-6-2-1-3-7-16/h1-9,17,23H,10-15H2

66307-47-9SDS

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-fluorophenoxy)-3-(4-phenylpiperazin-1-yl)propan-2-ol

1.2 Other means of identification

Product number -
Other names 1-(2-hydroxy-3-phenylpiperazinopropoxy)-2-fluorobenzene

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:66307-47-9 SDS

66307-47-9Downstream Products

66307-47-9Relevant academic research and scientific papers

Studies on new phosphodiesterase inhibitors. I. Synthesis of 1-(2,3-epoxypropoxy)-2(4)-fluorobenzenes and 1-(2-hydroxy-3-morpholinopropoxy and piperazino)fluorobenzene derivatives

Baker,Byrne,Economides,Javed

, p. 1045 - 1048 (2007/10/02)

A series of 1-(2,3-epoxypropoxy)-2(4)-fluorobenzenes and their corresponding 1-(2-hydroxy-3-morpholino propoxy and piperazino)fluorobenzene derivatives (8a-f) were synthesised via a short synthetic route in good chemical yields and were evaluated for inot

3-Tertiary amino-1-aryloxy- or aryl-propanes and -propan -2-ols and some related compounds

Gupta,Mukerji,Chatterjee,Rastogi,Anand,Dube,Sur Jr.,Mukerji,Srimal

, p. 241 - 246 (2007/10/04)

The synthesis and pharmacological activity of some 3 tertiary amino 1 aryloxy or 1 aryl, 1 thiophenoxy and 1 anilino propan 2 ols and propanes, particularly those derived from N phenylpiperazines are described. Effect of substituents (nature/position) on the phenyl ring, the phenoxy ring as well as alteration in the hydroxylic function vis a vis the structure activity relationships (SAR) are discussed. In general, the 1 aryloxy compounds have hypotensive activity this being more pronounced in those carrying an o substituent on the phenyl ring, while m and p substituted derivatives have their effect primarily on the CNS. Variations in the phenoxy moiety do not significantly alter the intrinsic activity. The 1 aryl compounds, on the other hand, have significant CNS activity, which is markedly affected by the substituents on the 1 aryl residue.

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