3-(Benzyloxy)-4-bromobenzoic acid

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Reagent Code: #140810
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CAS Number 17054-27-2

science Other reagents with same CAS 17054-27-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.1 g/mol
Formula C₁₄H₁₁BrO₃
thermostat Physical Properties
Melting Point 198-201 °C
Boiling Point 441.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.514±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive molecules and drug candidates. The benzyloxy group at the 3-position acts as a protecting group for the phenolic hydroxyl, while the bromine at the 4-position and carboxylic acid functional groups allow for further chemical modifications, such as cross-coupling reactions (e.g., Suzuki coupling) and esterification, making it valuable in building complex organic structures. Commonly employed in research settings for constructing benzodiazepine derivatives and other heterocyclic compounds with potential therapeutic activity, including anti-inflammatory and CNS-acting agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,090.00
inventory 1g
10-20 days ฿12,720.00
inventory 5g
10-20 days ฿45,160.00

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3-(Benzyloxy)-4-bromobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive molecules and drug candidates. The benzyloxy group at the 3-position acts as a protecting group for the phenolic hydroxyl, while the bromine at the 4-position and carboxylic acid functional groups allow for further chemical modifications, such as cross-coupling reactions (e.g., Suzuki coupling) and esterification, making it valuable in building complex organic structures. Commonly

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of bioactive molecules and drug candidates. The benzyloxy group at the 3-position acts as a protecting group for the phenolic hydroxyl, while the bromine at the 4-position and carboxylic acid functional groups allow for further chemical modifications, such as cross-coupling reactions (e.g., Suzuki coupling) and esterification, making it valuable in building complex organic structures. Commonly employed in research settings for constructing benzodiazepine derivatives and other heterocyclic compounds with potential therapeutic activity, including anti-inflammatory and CNS-acting agents.

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