Methyl2-bromo-2-(2-nitrophenyl)acetate

98%

Reagent Code: #213548
fingerprint
CAS Number 42794-41-2

science Other reagents with same CAS 42794-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2747 g/mol
Formula C₉H₈BrNO₄
badge Registry Numbers
MDL Number MFCD09037919
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through bromine displacement or nitro group reduction, enabling the construction of complex molecules. Commonly employed in the development of bioactive compounds due to the reactivity of the ester and nitro functionalities. Also utilized in photochemical studies where the nitroaryl group acts as a photolabile protecting group or photosensitizer.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,310.00
inventory 250mg
10-20 days ฿12,190.00
inventory 1g
10-20 days ฿29,950.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl2-bromo-2-(2-nitrophenyl)acetate
No image available

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through bromine displacement or nitro group reduction, enabling the construction of complex molecules. Commonly employed in the development of bioactive compounds due to the reactivity of the ester and nitro functionalities. Also utilized in photochemical studies where the nitroaryl group acts as a photolabile protecting group or

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through bromine displacement or nitro group reduction, enabling the construction of complex molecules. Commonly employed in the development of bioactive compounds due to the reactivity of the ester and nitro functionalities. Also utilized in photochemical studies where the nitroaryl group acts as a photolabile protecting group or photosensitizer.

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...