Methyl 4-(1-bromoethyl)benzoate

97%

Reagent Code: #207247
fingerprint
CAS Number 16281-97-3

science Other reagents with same CAS 16281-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.1 g/mol
Formula C₁₀H₁₁BrO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic structures. Its bromoethyl group allows for further functionalization through substitution or elimination reactions, making it valuable in pharmaceutical and agrochemical research. The ester moiety can be hydrolyzed to yield carboxylic acid derivatives, enabling incorporation into larger molecules. It is also employed in cross-coupling reactions to construct carbon-carbon bonds, useful in the development of functional materials and bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿1,740.00
inventory 5g
10-20 days ฿7,640.00
inventory 10g
10-20 days ฿15,260.00
inventory 25g
10-20 days ฿29,500.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 4-(1-bromoethyl)benzoate
No image available

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic structures. Its bromoethyl group allows for further functionalization through substitution or elimination reactions, making it valuable in pharmaceutical and agrochemical research. The ester moiety can be hydrolyzed to yield carboxylic acid derivatives, enabling incorporation into larger molecules. It is also employed in cross-coupling reactions to construct carbon-carbon bonds, useful

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic structures. Its bromoethyl group allows for further functionalization through substitution or elimination reactions, making it valuable in pharmaceutical and agrochemical research. The ester moiety can be hydrolyzed to yield carboxylic acid derivatives, enabling incorporation into larger molecules. It is also employed in cross-coupling reactions to construct carbon-carbon bonds, useful in the development of functional materials and bioactive compounds.

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...