tert-Butyl 4-(4-methylpiperazin-1-yl)benzylcarbamate

97%

Reagent Code: #145923
fingerprint
CAS Number 927676-52-6

science Other reagents with same CAS 927676-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.42 g/mol
Formula C₁₇H₂₇N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure incorporates a protected amine and a methylpiperazine moiety, making it valuable in medicinal chemistry for modifying solubility, bioavailability, and receptor binding properties. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. Also utilized in the construction of complex molecules via carbamate deprotection and subsequent coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 4-(4-methylpiperazin-1-yl)benzylcarbamate
No image available

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure incorporates a protected amine and a methylpiperazine moiety, making it valuable in medicinal chemistry for modifying solubility, bioavailability, and receptor binding properties. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. Also utilized in the construction of complex molecules via carbamate deprotection and subsequ

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure incorporates a protected amine and a methylpiperazine moiety, making it valuable in medicinal chemistry for modifying solubility, bioavailability, and receptor binding properties. Commonly employed in the preparation of kinase inhibitors and central nervous system agents. Also utilized in the construction of complex molecules via carbamate deprotection and subsequent coupling reactions.

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...