2-[4-(Bromomethyl)phenyl]propionic acid

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Reagent Code: #143422
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Alias 2-P-Bromomethylphenylpropionic acid
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CAS Number 111128-12-2

science Other reagents with same CAS 111128-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.1 g/mol
Formula C₁₀H₁₁BrO₂
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MDL Number MFCD02093445
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly profen derivatives. Its bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in medicinal chemistry for building more complex drug molecules. Commonly employed in the preparation of prodrugs and in structure-activity relationship studies to modify pharmacokinetic properties. Also utilized in the development of photoaffinity labels due to the reactivity of the bromide moiety under UV light, enabling biochemical target identification.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿270.00
inventory 25g
10-20 days ฿370.00
inventory 100g
10-20 days ฿920.00
inventory 500g
10-20 days ฿4,210.00
inventory 2.5kg
10-20 days ฿19,160.00

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2-[4-(Bromomethyl)phenyl]propionic acid
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Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly profen derivatives. Its bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in medicinal chemistry for building more complex drug molecules. Commonly employed in the preparation of prodrugs and in structure-activity relationship studies to modify pharmacokinetic properties. Also utilized in the development of photoaffinity labels due to the reactivity of the bromide

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly profen derivatives. Its bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in medicinal chemistry for building more complex drug molecules. Commonly employed in the preparation of prodrugs and in structure-activity relationship studies to modify pharmacokinetic properties. Also utilized in the development of photoaffinity labels due to the reactivity of the bromide moiety under UV light, enabling biochemical target identification.

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