N-Acetyl-4-Hydroxypiperidine

≥98%

Reagent Code: #217526
fingerprint
CAS Number 4045-22-1

science Other reagents with same CAS 4045-22-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18 g/mol
Formula C₇H₁₃NO₂
thermostat Physical Properties
Boiling Point 299.369ºC
inventory_2 Storage & Handling
Density 1.139 g/cm3
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and neuroprotective compounds. Its structure supports the creation of bioactive molecules due to the presence of both hydroxyl and acetyl-protected nitrogen functionalities, allowing selective chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, especially those targeting neurological disorders. Also utilized in the preparation of antioxidants and enzyme inhibitors due to the reactivity of the hydroxyl group and the stability of the acetylated piperidine ring.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,210.00
inventory 25g
10-20 days ฿11,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-Acetyl-4-Hydroxypiperidine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and neuroprotective compounds. Its structure supports the creation of bioactive molecules due to the presence of both hydroxyl and acetyl-protected nitrogen functionalities, allowing selective chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, especially those targeting neurological disorders. Also utilized

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and neuroprotective compounds. Its structure supports the creation of bioactive molecules due to the presence of both hydroxyl and acetyl-protected nitrogen functionalities, allowing selective chemical modifications. Commonly employed in medicinal chemistry for constructing piperidine-based drug candidates, especially those targeting neurological disorders. Also utilized in the preparation of antioxidants and enzyme inhibitors due to the reactivity of the hydroxyl group and the stability of the acetylated piperidine ring.

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...