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1-(4-Fluorophenyl)pentylamine is an organic compound with the molecular formula C11H16FN. It is a derivative of pentylamine, where one of the hydrogen atoms on the phenyl ring is replaced by a fluorine atom. This chemical is a colorless liquid with a density of 0.97 g/cm3 and a boiling point of 256°C. It is soluble in organic solvents and has a molecular weight of 179.25 g/mol. 1-(4-FLUOROPHENYL)PENTYLAMINE is primarily used as a building block in the synthesis of various pharmaceuticals and agrochemicals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other psychiatric medications. Due to its potential applications in the pharmaceutical industry, 1-(4-fluorophenyl)pentylamine is a subject of interest for researchers and chemists.

3823-26-5

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3823-26-5 Usage

Class

Substituted phenethylamines

Psychoactive effects

Known for their psychoactive effects

Structural components

Contains a 4-fluorophenyl group attached to a pentylamine chain

Potential applications

Medicinal chemistry and drug discovery

Structural similarity

Similarity to other bioactive compounds

Risks and adverse effects

Potential risks or adverse effects, should be handled and used with caution in laboratory or industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 3823-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,2 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3823-26:
(6*3)+(5*8)+(4*2)+(3*3)+(2*2)+(1*6)=85
85 % 10 = 5
So 3823-26-5 is a valid CAS Registry Number.

3823-26-5Relevant academic research and scientific papers

Synthesis of optically-active benzylic amines; asymmetric reduction of ketoxime ethers with chiral oxazaborolidines

Fontaine, Evelyne,Namane, Claudie,Meneyrol, Jerome,Geslin, Michel,Serva, Laurence,Roussey, Eliane,Tissandie, Stephanie,Maftouh, Mohamed,Roger, Pierre

, p. 2185 - 2189 (2001)

The preparation of novel optically active benzylic amines by the enantioselective reduction of phenone oximes using chiral oxazaborolidine is described. The choice of the chiral 1,2-amino alcohol (S)-diphenylvalinol as chiral inducer and that of the benzy

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