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4-ethylamphetamine

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EntityQ4637125· pop 5· linked from 6 articles

4-ethylamphetamine

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Also known as Ethylamphetamine, 4-EA, 1-(4-ethylphenyl)propan-2-amine

4-Ethylamphetamine (4-EA) is a substituted amphetamine derivative which has been sold as a designer drug. It is mainly known as a synthetic intermediate used as a building block to manufacture larger molecules, but 4-EA is closely related in chemical structure to designer drugs such as 4-methylamphetamine and 4-ethylmethcathinone, and is both a synthetic precursor and a metabolite of the 25-NB derivative 4-EA-NBOMe.

In the Vinony graph

Within Vinony's link graph, 4-ethylamphetamine is referenced by 6 other articles, and connects out to medication, nervous system and digital object identifier.

It is catalogued under topics including Chemical pages without DrugBank identifier, Drugs missing an ATC code and Infobox drug articles with non-default infobox title.

Its subject is documented across 4 Wikipedia language editions.

Chemical data

Formula
C11H17N
Molecular weight
163.26 g/mol
IUPAC name
1-(4-ethylphenyl)propan-2-amine
SMILES
CCC1=CC=C(C=C1)CC(C)N
InChIKey
VHFLVGIMDGXALR-UHFFFAOYSA-N
XLogP
2.5
Polar surface area
26 Ų
H-bond donors
1
H-bond acceptors
1
Formal charge
0

via PubChem

Wikidata facts

Mass
163.136099544
Show 3 more facts
chemical formula
C₁₁H₁₇N
Commons category
4-Ethylamphetamine
canonical SMILES
NC(C)Cc1ccc(cc1)CC

via Wikidata · CC0

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Encyclopedic overview

2 sections
Contents
  • See also
  • References

4-Ethylamphetamine (4-EA) is a substituted amphetamine derivative which has been sold as a designer drug. It is mainly known as a synthetic intermediate used as a building block to manufacture larger molecules, but 4-EA is closely related in chemical structure to designer drugs such as 4-methylamphetamine and 4-ethylmethcathinone, and is both a synthetic precursor and a metabolite of the 25-NB derivative 4-EA-NBOMe.

== See also == 25E-NBOMe 4-Et-PVP Amfepentorex DOET RTI-83

Excerpted from Wikipedia’s “4-ethylamphetamine” article, available under the CC BY-SA 4.0 licence.

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