(R)-2-((tert-Butoxycarbonyl)amino)-3-(furan-2-yl)propanoic acid

95%

Reagent Code: #37447
label
Alias Boc-D-2-Furylalanine.DCHA
fingerprint
CAS Number 261380-18-1

science Other reagents with same CAS 261380-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.27 g/mol
Formula C₁₂H₁₇NO₅
badge Registry Numbers
MDL Number MFCD01320879
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This allows for selective modifications to the molecule without unwanted side reactions. It is particularly valuable in the development of pharmaceuticals, where it can be incorporated into drug candidates targeting specific biological pathways. Additionally, its furan moiety can participate in further chemical transformations, making it a versatile building block in organic synthesis. Its applications extend to research in medicinal chemistry, where it aids in the creation of novel compounds with potential therapeutic effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,016.00
inventory 250mg
10-20 days ฿4,086.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-((tert-Butoxycarbonyl)amino)-3-(furan-2-yl)propanoic acid
No image available

This compound is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This allows for selective modifications to the molecule without unwanted side reactions. It is particularly valuable in the development of pharmaceuticals, where it can be incorporated into drug candidates targeting specific biological pathways. Additiona

This compound is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This allows for selective modifications to the molecule without unwanted side reactions. It is particularly valuable in the development of pharmaceuticals, where it can be incorporated into drug candidates targeting specific biological pathways. Additionally, its furan moiety can participate in further chemical transformations, making it a versatile building block in organic synthesis. Its applications extend to research in medicinal chemistry, where it aids in the creation of novel compounds with potential therapeutic effects.

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...