Methyl 4-(bromomethyl)benzoate

98.0%

Reagent Code: #205257
label
Alias Methyl p-benzoate; α-Bromo-P-Toluene Methyl Ester
fingerprint
CAS Number 2417-72-3

science Other reagents with same CAS 2417-72-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula C₉H₉BrO₂
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD00032453
thermostat Physical Properties
Melting Point 57-58 °C(lit.)
Boiling Point 130-135 °C2 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.47 g/cm3
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation or substitution reactions, making it valuable for introducing aromatic ester moieties into larger molecules. Commonly employed in the synthesis of liquid crystals, functionalized polymers, and bioactive compounds where a methyl benzoate scaffold is required. Also utilized in cross-coupling reactions and as a building block in medicinal chemistry for constructing drug-like molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿310.00
25g
10-20 days ฿1,480.00
100g
10-20 days ฿5,790.00
500g
10-20 days ฿28,810.00
Methyl 4-(bromomethyl)benzoate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation or substitution reactions, making it valuable for introducing aromatic ester moieties into larger molecules. Commonly employed in the synthesis of liquid crystals, functionalized polymers, and bioactive compounds where a methyl benzoate scaffold is required. Also utilized in cross-coupling reactions and as a building block in medi

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromomethyl group allows for easy alkylation or substitution reactions, making it valuable for introducing aromatic ester moieties into larger molecules. Commonly employed in the synthesis of liquid crystals, functionalized polymers, and bioactive compounds where a methyl benzoate scaffold is required. Also utilized in cross-coupling reactions and as a building block in medicinal chemistry for constructing drug-like molecules.

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