4-Amino-1-Boc-piperidine

97%

Reagent Code: #134950
label
Alias 4-amino-1-tert-butoxycarbonylpiperidine 1-Tert-butoxycarbonyl-4-aminopiperidine 1-Boc-4-aminopiperidine
fingerprint
CAS Number 87120-72-7

science Other reagents with same CAS 87120-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD01076201
thermostat Physical Properties
Melting Point 50°C
Boiling Point 80/0.037mm
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), especially in the development of drugs targeting central nervous system disorders. Its protected amine group allows for selective reactions, making it valuable in multi-step organic syntheses. It is frequently employed in the preparation of protease inhibitors, receptor agonists, and antagonists. Due to the Boc (tert-butoxycarbonyl) protecting group, it enables mild deprotection conditions, which helps preserve sensitive functional groups in complex molecules. It is also utilized in combinatorial chemistry and medicinal chemistry research for constructing piperidine-based drug candidates.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 42-48
Purity (GC) 97-100
APPEARANCE White to Yellow Powder, Crystals, Crystalline Powder and/or Chunks
INFRARED SPECTRUM Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿260.00
5g
10-20 days ฿330.00
25g
10-20 days ฿1,190.00
100g
10-20 days ฿4,460.00
500g
10-20 days ฿21,870.00
4-Amino-1-Boc-piperidine
No image available

Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), especially in the development of drugs targeting central nervous system disorders. Its protected amine group allows for selective reactions, making it valuable in multi-step organic syntheses. It is frequently employed in the preparation of protease inhibitors, receptor agonists, and antagonists. Due to the Boc (tert-butoxycarbonyl) protecting group, it enables mild

Widely used in pharmaceutical synthesis, this compound serves as a key building block for creating active pharmaceutical ingredients (APIs), especially in the development of drugs targeting central nervous system disorders. Its protected amine group allows for selective reactions, making it valuable in multi-step organic syntheses. It is frequently employed in the preparation of protease inhibitors, receptor agonists, and antagonists. Due to the Boc (tert-butoxycarbonyl) protecting group, it enables mild deprotection conditions, which helps preserve sensitive functional groups in complex molecules. It is also utilized in combinatorial chemistry and medicinal chemistry research for constructing piperidine-based drug candidates.

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...