tert-butyl ((1-(3,4,5-trimethoxyphenyl)cyclobutyl)methyl)carbamate

90%

Reagent Code: #241959

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.44 g/mol
Formula C₁₉H₂₉NO₅
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a protected intermediate in pharmaceutical synthesis, featuring a cyclobutane ring substituted with a 3,4,5-trimethoxyphenyl group and a tert-butyl carbamate on the aminomethyl side chain. This structure is valuable for developing central nervous system-active compounds, particularly anti-inflammatory and analgesic agents. The tert-butyl carbamate protecting group shields the amine during multi-step reactions, improving reaction specificity and compound stability under harsh conditions, while facilitating the creation of bioactive molecules with enhanced pharmacokinetic profiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,880.00
inventory 250mg
10-20 days ฿8,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-butyl ((1-(3,4,5-trimethoxyphenyl)cyclobutyl)methyl)carbamate
No image available

Used as a protected intermediate in pharmaceutical synthesis, featuring a cyclobutane ring substituted with a 3,4,5-trimethoxyphenyl group and a tert-butyl carbamate on the aminomethyl side chain. This structure is valuable for developing central nervous system-active compounds, particularly anti-inflammatory and analgesic agents. The tert-butyl carbamate protecting group shields the amine during multi-step reactions, improving reaction specificity and compound stability under harsh conditions, while fac

Used as a protected intermediate in pharmaceutical synthesis, featuring a cyclobutane ring substituted with a 3,4,5-trimethoxyphenyl group and a tert-butyl carbamate on the aminomethyl side chain. This structure is valuable for developing central nervous system-active compounds, particularly anti-inflammatory and analgesic agents. The tert-butyl carbamate protecting group shields the amine during multi-step reactions, improving reaction specificity and compound stability under harsh conditions, while facilitating the creation of bioactive molecules with enhanced pharmacokinetic profiles.

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...