1-(tert-Butoxycarbonyl)-3-methylpiperidine-3-carboxylic acid

97%

Reagent Code: #145965
fingerprint
CAS Number 534602-47-6

science Other reagents with same CAS 534602-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.3 g/mol
Formula C₁₂H₂₁NO₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine group and carboxylic acid functionality make it valuable in peptide coupling and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing modulators of central nervous system targets and kinase inhibitors. The Boc-protected amine allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex molecules in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿820.00
inventory 5g
10-20 days ฿2,880.00
inventory 25g
10-20 days ฿13,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(tert-Butoxycarbonyl)-3-methylpiperidine-3-carboxylic acid
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine group and carboxylic acid functionality make it valuable in peptide coupling and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing modulators of central nervous system targets and kinase inhibitors. The Boc-protected amine allows for selective deprotection under mild acidic c

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine group and carboxylic acid functionality make it valuable in peptide coupling and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing modulators of central nervous system targets and kinase inhibitors. The Boc-protected amine allows for selective deprotection under mild acidic conditions, enabling stepwise assembly of complex molecules in multi-step syntheses.

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...