Di-tert-butyl (S)-2-(aminomethyl)piperazine-1,4-dicarboxylate

98%

Reagent Code: #178438
fingerprint
CAS Number 1808248-63-6

science Other reagents with same CAS 1808248-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.4085 g/mol
Formula C₁₅H₂₉N₃O₄
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. It features a piperazine core with N1 and N4 protected by tert-butoxycarbonyl (Boc) groups and a free aminomethyl side chain at the (S)-2 position, making it valuable in medicinal chemistry for constructing peptidomimetics and kinase inhibitors. Commonly employed in solid-phase and solution-phase peptide synthesis due to the orthogonal protecting groups that allow selective deprotection and coupling. Also utilized in the preparation of protease inhibitors and GPCR-targeted compounds where the piperazine scaffold enhances solubility and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,880.00
inventory 100mg
10-20 days ฿13,630.00
inventory 250mg
10-20 days ฿20,440.00
inventory 1g
10-20 days ฿62,720.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Di-tert-butyl (S)-2-(aminomethyl)piperazine-1,4-dicarboxylate
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. It features a piperazine core with N1 and N4 protected by tert-butoxycarbonyl (Boc) groups and a free aminomethyl side chain at the (S)-2 position, making it valuable in medicinal chemistry for constructing peptidomimetics and kinase inhibitors. Commonly employed in solid-phase and solution-phase peptide synthesis due to the orth

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. It features a piperazine core with N1 and N4 protected by tert-butoxycarbonyl (Boc) groups and a free aminomethyl side chain at the (S)-2 position, making it valuable in medicinal chemistry for constructing peptidomimetics and kinase inhibitors. Commonly employed in solid-phase and solution-phase peptide synthesis due to the orthogonal protecting groups that allow selective deprotection and coupling. Also utilized in the preparation of protease inhibitors and GPCR-targeted compounds where the piperazine scaffold enhances solubility and binding affinity.

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...