Fluphenazine enanthate

Base Information

• Chemical Name: Fluphenazine enanthate
• CAS No.: 2746-81-8
• Molecular Formula: C29H38 F3 N3 O2 S
• Molecular Weight: 549.701
• European Community (EC) Number: 220-385-0
• UNII: QSB34YF0W9
• DSSTox Substance ID: DTXSID6023070
• Nikkaji Number: J7.903K
• Wikidata: Q27106667
• NCI Thesaurus Code: C65726
• Pharos Ligand ID: FQV44DLKAPSW,Z378NHVBMRZD
• Metabolomics Workbench ID: 67451
• ChEMBL ID: CHEMBL1200951
• Mol file: 2746-81-8.mol

Synonyms:fluphenazine enanthate;Moditen enanthate

Chemical Property of Fluphenazine enanthate

Chemical Property:

• Vapor Pressure: 9.41E-16mmHg at 25°C
• Melting Point: 184.5°C
• Boiling Point: 629.4°Cat760mmHg
• PKA: 7.32±0.10(Predicted)
• Flash Point: 334.4°C
• PSA: 61.32000
• Density: 1.181g/cm³
• LogP: 6.77020
• Solubility.: Practically insoluble in water, very soluble in ethanol and in methylene chloride, freely soluble in methanol.
• XLogP3: 7.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 13
• Exact Mass: 549.26368312
• Heavy Atom Count: 38
• Complexity: 720

Purity/Quality:

98%Min ^*data from raw suppliers

Fluphenazine enantate European Pharmacopoeia (EP) Reference Standard ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC(=O)OCCN1CCN(CC1)CCCN2C3=CC=CC=C3SC4=C2C=C(C=C4)C(F)(F)F
• Uses: Fluphenazine Enanthate serves as a medication for the treatment of tardive dyskinesia (TD) in monkeys. Fluphenazine Enanthate also functions as a medication for the antipsychotics study on human prolactin levels. Fluphenazine Enanthate reduces the blood pressure of pentobarbital Na anesthetized dogs, reduces heart rate in anesthetized dogs, and increases coronary blood flow and femoral blood flow in anesthetized dogs enhancing cardiovascular functions. Antipsychotic.

Technology Process of Fluphenazine enanthate

There total 1 articles about Fluphenazine enanthate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ fluphenazine enanthate (2746-81-8)

Guidance literature:

4-<3-(2-Trifluormethyl-phenothiazinyl-(10))-propyl>-1-(2-hydroxy-ethyl)-piperazin, Heptanoylchlorid; analog entstehen 14C-haltige Praeparate aus Heptanoylchlorid und der entspr. 14C-haltigen Substanz;

DOI:10.1021/jm00340a002

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