| Weight | 167.277 g/mol |
|---|---|
| Formula | C9H13NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-thien-2-ylpiperidine (198334-38-2)
4-(2-thienyl)piperidine · 198334-38-2
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- [3H]N-[1-(2-Thienyl)cyclohexyl]-3,4-Piperidine ([3H]TCP) Binding in Human Frontal Cortex: Decreases in Alzheimer-Type Dementia (Journal of Neurochemistry, 1990)
- A comparison of [3H]MK-801 and N-[1-(2-thienyl)cyclohexyl]-3,4-[3H]piperidine binding to the N-methyl-D-aspartate receptor complex in human brain. (Journal of Neurochemistry, 1991)
- Synthesis of high specific activity (3,4-[3H]cyclohexyl)-N-[1 (2-benzo[b]thienyl)cyclohexyl]piperidine {[3H]BTCP}: A selective probe for the dopamine-reuptake complex (Journal of Labelled Compounds and Radiopharmaceuticals, 1991)
- Biphasic effects of magnesium on the [3H]N-(1-(2-thienyl)cyclohexyl)-3,4-piperidine binding in the rat cerebral cortex (Neuroscience Letters, 1990)
- Effects of the major metabolite of phencyclidine, the trans isomer of 4-phenyl-4-(1-piperidinyl)cyclohexanol, on [3H]N-(1-[2-thienyl] cyclohexyl)-3,4-piperidine ([3H]TCP) binding and [3H]dopamine uptake in the rat brain. (Neuroscience Letters, 1994)
- Positron labeled analogs of TCP: Synthesis of 1[4[18F]fluoromethyl-1(2-thienyl)cyclohexyl]piperidine (International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-(2-thienyl)piperidine
- 198334-38-2
-
SMILESC1CNCCC1C2=CC=CS2
-
InChIKeySLQVNTKKWCOXKW-UHFFFAOYSA-N
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Safety
Alternate Names
Estimated Properties
| Boiling Point | 238.81 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 273.9 C | EPI Suite |
| Density | 1.07 g/cm3 | EPA T.E.S.T. |
| Flash Point | 98 C | EPA T.E.S.T. |
| Melting Point | 68.97 C | EPI Suite |
| Water Solubility | 408.18 mg/L | EPA T.E.S.T. |
| Water Solubility | 8602.8 mg/L | EPI Suite |
External Links
Synthesis
3-(2-Thienyl)butylamine
+
Reactant
(Alkylation of primary amines)
Reactant
+
3-(Thiophen-2-yl)propan-1-amine
(Reductive amination)
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4-thien-2-ylpiperidine
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