| Weight | 147.221 g/mol |
|---|---|
| Formula | C10H13N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1,2,3,4-tetrahydronaphthalen-2-amine (2954-50-9)
2954-50-9 · 1,2,3,4-tetrahydro-2-naphthalenamine
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- Sigma-Aldrich - Search for 1,2,3,4-tetrahydronaphthalen-2-amine
- Fisher Scientific - Search for 1,2,3,4-tetrahydronaphthalen-2-amine
- TCI - Search for 1,2,3,4-tetrahydronaphthalen-2-amine
- Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine (1979)
- A New and Simplified Process for Preparing N-[4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine and a Telescoped Process for the Synthesis of (1S-cis)-4-(3,4-Dichlorophenol)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine Mandelate: Key Intermediates in the Synthesis of Sertraline Hydrochloride (Organic Process Research & Development, 2004)
- Antidepressant derivatives of trans-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine (1980)
- l-1,2,3,4-Tetrahydro-8-methoxy-5-(methylthio)-2-naphthalenamine: a potent and selective agonist at alpha 1-adrenoceptors. (Journal of Medicinal Chemistry, 1983)
- Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine and pharmaceutical compositions thereof (1980)
- Antidepressant derivatives of trans-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine and pharmaceutical compositions thereof (1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2954-50-9
- 1,2,3,4-tetrahydro-2-naphthalenamine
-
SMILESC1CC2=CC=CC=C2CC1N
-
InChIKeyLCGFVWKNXLRFIF-UHFFFAOYSA-N
- Pubchem - 1,2,3,4-tetrahydronaphthalen-2-amine
- Wikipedia - 1,2,3,4-tetrahydronaphthalen-2-amine
2-Aminotetralin (2-AT), also known as 1,2,3,4-tetrahydronaphthalen-2-amine (THN), is a stimulant drug with a chemical structure consisting of a tetralin group combined with an amine. 2-AT is a rigid analogue of phenylisobutylamine and fully substitutes for d-amphetamine in rat discrimination tests, although at one eighth the potency. It has been shown to inhibit the reuptake of serotonin and norepinephrine, and likely induces their release as well.
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