(S)-tert-Butyl 4-(2-aminopropyl)piperazine-1-carboxylate

95%

Reagent Code: #234942
fingerprint
CAS Number 1017606-58-4

science Other reagents with same CAS 1017606-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.35 g/mol
Formula C₁₂H₂₅N₃O₂
badge Registry Numbers
MDL Number MFCD18249855
thermostat Physical Properties
Boiling Point 330.0±32.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure supports the creation of selective serotonin and dopamine modulators, making it valuable in the production of antidepressants and antipsychotics. The tert-butyloxycarbonyl (Boc) protecting group allows for controlled deprotection during multi-step syntheses, enhancing reaction specificity. Commonly employed in medicinal chemistry for building complex piperazine-based molecules with improved bioavailability and target binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,640.00
inventory 250mg
10-20 days ฿4,950.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-tert-Butyl 4-(2-aminopropyl)piperazine-1-carboxylate
No image available

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure supports the creation of selective serotonin and dopamine modulators, making it valuable in the production of antidepressants and antipsychotics. The tert-butyloxycarbonyl (Boc) protecting group allows for controlled deprotection during multi-step syntheses, enhancing reaction specificity. Commonly employed in medicinal chemistry for building co

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure supports the creation of selective serotonin and dopamine modulators, making it valuable in the production of antidepressants and antipsychotics. The tert-butyloxycarbonyl (Boc) protecting group allows for controlled deprotection during multi-step syntheses, enhancing reaction specificity. Commonly employed in medicinal chemistry for building complex piperazine-based molecules with improved bioavailability and target 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...