4-(Oxolan-3-yl)piperidine hydrochloride

97%

Reagent Code: #222231
fingerprint
CAS Number 1461708-70-2

science Other reagents with same CAS 1461708-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.70 g/mol
Formula C₉H₁₈ClNO
badge Registry Numbers
MDL Number MFCD25371829
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of central nervous system agents. Its structure supports the design of compounds with neurological activity, including potential use in antidepressants and receptor modulators. Commonly employed in medicinal chemistry for scaffold development due to its piperidine ring substituted at the 4-position with a tetrahydrofuran-3-yl moiety, enhancing binding selectivity. Also utilized in the preparation of novel drug candidates targeting pain management and cognitive disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,200.00
inventory 250mg
10-20 days ฿21,910.00
inventory 1g
10-20 days ฿70,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(Oxolan-3-yl)piperidine hydrochloride
No image available

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of central nervous system agents. Its structure supports the design of compounds with neurological activity, including potential use in antidepressants and receptor modulators. Commonly employed in medicinal chemistry for scaffold development due to its piperidine ring substituted at the 4-position with a tetrahydrofuran-3-yl moiety, enhancing binding selectivity. Also utilized in the pr

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of central nervous system agents. Its structure supports the design of compounds with neurological activity, including potential use in antidepressants and receptor modulators. Commonly employed in medicinal chemistry for scaffold development due to its piperidine ring substituted at the 4-position with a tetrahydrofuran-3-yl moiety, enhancing binding selectivity. Also utilized in the preparation of novel drug candidates targeting pain management and cognitive disorders.

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...