Boc-D-Phg(3,5-F2)-OH

97%

Reagent Code: #37396
fingerprint
CAS Number 1241677-76-8

science Other reagents with same CAS 1241677-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.26 g/mol
Formula C₁₃H₁₅F₂NO₄
badge Registry Numbers
MDL Number MFCD07371827
thermostat Physical Properties
Boiling Point 398.7±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It is particularly valuable in the preparation of complex peptides and proteins where selective protection and deprotection of functional groups are required. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing for controlled reactions during peptide chain assembly. The presence of fluorine atoms on the phenyl ring can enhance the biological activity or stability of the resulting peptides, making it useful in the development of pharmaceutical compounds, especially those targeting specific enzymes or receptors. Additionally, it is employed in research settings to study peptide structure-activity relationships and to design novel bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,331.00
inventory 100mg
10-20 days ฿10,161.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Boc-D-Phg(3,5-F2)-OH
No image available
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It is particularly valuable in the preparation of complex peptides and proteins where selective protection and deprotection of functional groups are required. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing for controlled reactions during peptide chain assembly. The presence of fluorine atoms on the phenyl ring can enhance the biological activity or stability of t
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It is particularly valuable in the preparation of complex peptides and proteins where selective protection and deprotection of functional groups are required. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing for controlled reactions during peptide chain assembly. The presence of fluorine atoms on the phenyl ring can enhance the biological activity or stability of the resulting peptides, making it useful in the development of pharmaceutical compounds, especially those targeting specific enzymes or receptors. Additionally, it is employed in research settings to study peptide structure-activity relationships and to design novel bioactive molecules.
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...