| Identification | Back Directory | [Name]
BTCP HCL | [CAS]
112726-66-6 | [Synonyms]
gk13
GK 1
BTCP HCL
Benocyclidine
Benocyclidine hydrochloride
112726-66-6 BTCP HCL C19H25NS
BTCP HYDROCHLORIDE POTENT & SELECTIVE DO
Benzothiophenylcyclohexylpiperidine Maleate
1-(1-benzo(b)thien-2-ylcyclohexyl)-piperidin
1-(1-benzo(b)thien-2-ylcyclohexyl)piperidine
1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine
Piperidine,1-(1-benzo[b]thien-2-ylcyclohexyl)-
1-(1-Benzo[b]thiophen-2-ylcyclohexyl)piperidine
1-[1-(1-Benzothiophen-2-yl)cyclohexyl]piperidine
N-[1-(2-Benzo[b]thiophenyl)cyclohexyl]piperidine
1-[1-(1-benzothiophen-2-yl)cyclohexyl]piperidine Maleate
N-[1-(Benzo[b]thien-2-yl-cyclohexyl)]piperidine hydrochloride | [Molecular Formula]
C19H25NS | [MDL Number]
MFCD00153777 | [MOL File]
112726-66-6.mol | [Molecular Weight]
299.47 |
| Chemical Properties | Back Directory | [Melting point ]
80℃ (ethanol ) | [Boiling point ]
425.4±20.0 °C(Predicted) | [density ]
1.135±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
H2O: >180 mg/mL | [form ]
solid | [pka]
8.56±0.20(Predicted) | [color ]
white |
| Hazard Information | Back Directory | [Uses]
Benzothiophenylcyclohexylpiperidine Maleate is a potent dopamine re-uptake/transport inhibitor different from PCP and other stimulants. | [Definition]
ChEBI: A tertiary amino compound that consists of cyclohexane having piperidin-1-yl and benzothiophen-2-yl groups attached at position 1. A potent dopamine re-uptake inhibitor with a behavioral profile different from that of phencyclidine (PCP) and similar to tha
of cocaine. | [Biological Activity]
A potent dopamine re-uptake inhibitor with a behavioral profile different from that of PCP and similar to that of cocaine. | [References]
[1] vignon j, pinet v, cerruti c, et al. [3h] n-[1-(2-benzo (b) thiophenyl) cycohexyl] piperidine ([3h] btcp): a new phencyclidine analog selective for the dopamine uptake complex[j]. european journal of pharmacology, 1988, 148(3): 427-436.
[2] chaudieu i, vignon j, chicheportiche m, et al. role of the aromatic group in the inhibition of phencyclidine binding and dopamine uptake by pcp analogs[j]. pharmacology biochemistry and behavior, 1989, 32(3): 699-705.
[3] seeman p. brain dopamine receptors[j]. pharmacological reviews, 1980, 32(3): 229-313.
[4] maurice t, vignon j, kamenka j m, et al. in vivo labelling of the mouse dopamine uptake complex with the phencyclidine derivative [3 h] btcp[j]. neuroscience letters, 1989, 101(2): 234-238. |
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Sinfachem Limited.
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025-84683399 13952017251 |
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http://www.sinfachem.com |
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