tert-butyl (2-(2-(2-hydroxyethoxy)ethoxy)ethyl)carbamate

97%

Reagent Code: #145583
fingerprint
CAS Number 139115-92-7

science Other reagents with same CAS 139115-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.31 g/mol
Formula C₁₁H₂₃NO₅
thermostat Physical Properties
Boiling Point 374.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a protected amino alcohol building block in organic synthesis, particularly in pharmaceutical and medicinal chemistry. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine for further transformations. The triethylene glycol-like linker imparts water solubility and flexibility, making it valuable in the design of drug conjugates, prodrugs, and polyethylene glycol (PEG)-like spacers. Commonly employed in the synthesis of complex molecules where a hydrophilic, protected amine handle is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿350.00
100mg
10-20 days ฿570.00
250mg
10-20 days ฿660.00
5g
10-20 days ฿5,380.00
25g
10-20 days ฿16,150.00
1g
10-20 days ฿1,330.00
tert-butyl (2-(2-(2-hydroxyethoxy)ethoxy)ethyl)carbamate
No image available

Used as a protected amino alcohol building block in organic synthesis, particularly in pharmaceutical and medicinal chemistry. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine for further transformations. The triethylene glycol-like linker imparts water solubility and flexibility, making it valuable in the design of drug conjugates, prodrugs, and polyethylene glycol (PEG)-like spacers. Commonly employed in

Used as a protected amino alcohol building block in organic synthesis, particularly in pharmaceutical and medicinal chemistry. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine for further transformations. The triethylene glycol-like linker imparts water solubility and flexibility, making it valuable in the design of drug conjugates, prodrugs, and polyethylene glycol (PEG)-like spacers. Commonly employed in the synthesis of complex molecules where a hydrophilic, protected amine handle is required.

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...