(±)-3-(Boc-aminomethyl)piperidine

98%

Reagent Code: #143460
label
Alias (±)-3-(Boc-aminomethyl)piperidine N-(3-piperidinylmethyl)carbamate tert-butyl 3-Boc-aminomethylpiperidine
fingerprint
CAS Number 142643-29-6

science Other reagents with same CAS 142643-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD01632454
thermostat Physical Properties
Melting Point 60-70 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where a piperidine scaffold is required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical flexibility and ease of derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿500.00
inventory 5g
10-20 days ฿4,150.00
inventory 25g
10-20 days ฿12,510.00
inventory 1g
10-20 days ฿1,650.00
(±)-3-(Boc-aminomethyl)piperidine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where a piperidine scaffold is required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules. Widely utilized in medicinal chemistry for structure-activity relatio

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where a piperidine scaffold is required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of kinase inhibitors, CNS-active compounds, and other bioactive molecules. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical flexibility and ease of derivatization.

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...