N-4-Piperidinyl-3-thiophenecarboxamidehydrochloride

97%

Reagent Code: #219603
fingerprint
CAS Number 1185314-33-3

science Other reagents with same CAS 1185314-33-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.76 g/mol
Formula C₁₀H₁₅ClN₂OS
badge Registry Numbers
MDL Number MFCD08752710
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Shows potential in the design of receptor ligands due to its structural affinity for neurological targets. Also employed in the preparation of antipsychotic and analgesic compounds, leveraging the piperidine and thiophene moieties for enhanced binding selectivity. Its hydrochloride salt form improves solubility and stability in formulation studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿32,600.00
N-4-Piperidinyl-3-thiophenecarboxamidehydrochloride
No image available

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Shows potential in the design of receptor ligands due to its structural affinity for neurological targets. Also employed in the preparation of antipsychotic and analgesic compounds, leveraging the piperidine and thiophene moieties for enhanced binding selectivity. Its hydrochloride salt form improves solubility and stability in formulation studie

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Shows potential in the design of receptor ligands due to its structural affinity for neurological targets. Also employed in the preparation of antipsychotic and analgesic compounds, leveraging the piperidine and thiophene moieties for enhanced binding selectivity. Its hydrochloride salt form improves solubility and stability in formulation studies.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...