2-((tert-Butoxycarbonyl)amino)-4,5-dimethoxybenzoic acid

97%

Reagent Code: #152176
fingerprint
CAS Number 122744-78-9

science Other reagents with same CAS 122744-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.30 g/mol
Formula C₁₄H₁₉NO₆
badge Registry Numbers
MDL Number MFCD02682186
thermostat Physical Properties
Boiling Point 378.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of complex organic molecules requiring selective protection of amine groups. Its carboxylic acid and protected amine functionalities allow for sequential coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, enabling controlled deprotection when needed. Commonly employed in the preparation of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,470.00
inventory 1g
10-20 days ฿9,340.00
inventory 5g
10-20 days ฿35,380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-((tert-Butoxycarbonyl)amino)-4,5-dimethoxybenzoic acid
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of complex organic molecules requiring selective protection of amine groups. Its carboxylic acid and protected amine functionalities allow for sequential coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, enabling controlled deprotection when needed. Commonly employed in the prepara

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of complex organic molecules requiring selective protection of amine groups. Its carboxylic acid and protected amine functionalities allow for sequential coupling reactions, making it valuable in peptide synthesis and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, enabling controlled deprotection when needed. Commonly employed in the preparation of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders.

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...