4-Nitrophenyl ethylcarbamate

97%

Reagent Code: #130424
fingerprint
CAS Number 17576-41-9

science Other reagents with same CAS 17576-41-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.19 g/mol
Formula C₉H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD01738228
thermostat Physical Properties
Boiling Point 329.1±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.279±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for amines due to its stability under various reaction conditions and selective deprotection properties. Also employed in the preparation of enzyme inhibitors and bioactive molecules, where the nitrophenyl group acts as a chromophore for easy monitoring of reactions. Its carbamate functionality makes it useful in the construction of urethane-based compounds with specific biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿12,980.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Nitrophenyl ethylcarbamate
No image available

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for amines due to its stability under various reaction conditions and selective deprotection properties. Also employed in the preparation of enzyme inhibitors and bioactive molecules, where the nitrophenyl group acts as a chromophore for easy monitoring of reactions. Its carbamate functionality makes it useful in the construction of urethane-based com

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for amines due to its stability under various reaction conditions and selective deprotection properties. Also employed in the preparation of enzyme inhibitors and bioactive molecules, where the nitrophenyl group acts as a chromophore for easy monitoring of reactions. Its carbamate functionality makes it useful in the construction of urethane-based compounds with specific biological activity.

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...