Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate

95%

Reagent Code: #182663
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CAS Number 1080026-94-3

science Other reagents with same CAS 1080026-94-3

blur_circular Chemical Specifications

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Weight 211.28 g/mol
Formula C₁₀H₁₃NO₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate is a key intermediate in the synthesis of Pramipexole, a non-ergoline dopamine agonist used for treating Parkinson's disease and restless legs syndrome. It functions as a building block for pharmaceuticals targeting central nervous system dopaminergic pathways, particularly D2 and D3 receptors. The bicyclic thienopyridine core with the ethyl carboxylate substituent enables selective modifications to optimize receptor affinity, pharmacokinetics, and blood-brain barrier penetration. Widely used in medicinal chemistry for structure-activity relationship (SAR) studies and development of novel CNS therapeutics.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,690.00
inventory 100mg
10-20 days ฿4,320.00
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Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate
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Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate is a key intermediate in the synthesis of Pramipexole, a non-ergoline dopamine agonist used for treating Parkinson's disease and restless legs syndrome. It functions as a building block for pharmaceuticals targeting central nervous system dopaminergic pathways, particularly D2 and D3 receptors. The bicyclic thienopyridine core with the ethyl carboxylate substituent enables selective modifications to optimize receptor affinity, pharmacokinetics,

Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate is a key intermediate in the synthesis of Pramipexole, a non-ergoline dopamine agonist used for treating Parkinson's disease and restless legs syndrome. It functions as a building block for pharmaceuticals targeting central nervous system dopaminergic pathways, particularly D2 and D3 receptors. The bicyclic thienopyridine core with the ethyl carboxylate substituent enables selective modifications to optimize receptor affinity, pharmacokinetics, and blood-brain barrier penetration. Widely used in medicinal chemistry for structure-activity relationship (SAR) studies and development of novel CNS therapeutics.

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