Methyl4-((tert-butoxycarbonyl)amino)-3-methoxybenzoate

98%

Reagent Code: #214164
fingerprint
CAS Number 941715-64-6

science Other reagents with same CAS 941715-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.30 g/mol
Formula C₁₄H₁₉NO₅
badge Registry Numbers
MDL Number MFCD24469321
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex drug candidates, especially those targeting cancer and inflammatory diseases. The Boc-protected amine ensures stability during reactions, while the methoxy and ester groups serve as handles for further modification.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿15,290.00
Methyl4-((tert-butoxycarbonyl)amino)-3-methoxybenzoate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex drug candidates, especially those targeting cancer and inflammatory diseases. The Boc-protected amine ensures stability during reactions, while the methoxy and ester groups serve a

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex drug candidates, especially those targeting cancer and inflammatory diseases. The Boc-protected amine ensures stability during reactions, while the methoxy and ester groups serve as handles for further modification.

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...