(S)-Methyl 2-((tert-butoxycarbonyl)amino)-2-(4-hydroxyphenyl)acetate

98%

Reagent Code: #38082
fingerprint
CAS Number 225517-15-7

science Other reagents with same CAS 225517-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.3100 g/mol
Formula C₁₄H₁₉NO₅
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a Boc-protected amino group and a hydroxyphenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the preparation of peptidomimetics and other bioactive molecules, where the chiral center and functional groups play a critical role in biological activity. Additionally, it serves as a precursor in the production of compounds targeting neurological and inflammatory disorders, leveraging its ability to interact with specific biological receptors. Its application is also seen in asymmetric synthesis, where it aids in creating enantiomerically pure substances for advanced drug development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,830.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Methyl 2-((tert-butoxycarbonyl)amino)-2-(4-hydroxyphenyl)acetate
No image available

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a Boc-protected amino group and a hydroxyphenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the preparation of peptidomimetics and other bioactive molecules, where the chiral center and functional groups play a critical role in biological activity. Additionally, it serves as a precursor in the production

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a Boc-protected amino group and a hydroxyphenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the preparation of peptidomimetics and other bioactive molecules, where the chiral center and functional groups play a critical role in biological activity. Additionally, it serves as a precursor in the production of compounds targeting neurological and inflammatory disorders, leveraging its ability to interact with specific biological receptors. Its application is also seen in asymmetric synthesis, where it aids in creating enantiomerically pure substances for advanced drug development.

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...