Ethyl 4-bromo-3-hydroxybutanoate

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Reagent Code: #184700
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CAS Number 32224-01-4

science Other reagents with same CAS 32224-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.05 g/mol
Formula C₆H₁₁BrO₃
badge Registry Numbers
MDL Number MFCD24390149
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-hydroxy ester derivatives which serve as building blocks for drugs such as cholesterol-lowering agents (statins). Its functional groups—bromine and hydroxyl—allow for selective chemical modifications, enabling the construction of complex molecular structures. Commonly employed in asymmetric synthesis to introduce chiral centers, it plays a role in the development of biologically active compounds, including antiviral and anti-inflammatory agents. Also utilized in the preparation of prodrugs due to the ester moiety, which can improve bioavailability.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿25,550.00
inventory 10g
10-20 days ฿32,300.00
inventory 25g
10-20 days ฿47,500.00

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Ethyl 4-bromo-3-hydroxybutanoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-hydroxy ester derivatives which serve as building blocks for drugs such as cholesterol-lowering agents (statins). Its functional groups—bromine and hydroxyl—allow for selective chemical modifications, enabling the construction of complex molecular structures. Commonly employed in asymmetric synthesis to introduce chiral centers, it plays a role in the development of biologically active compounds, includ

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-hydroxy ester derivatives which serve as building blocks for drugs such as cholesterol-lowering agents (statins). Its functional groups—bromine and hydroxyl—allow for selective chemical modifications, enabling the construction of complex molecular structures. Commonly employed in asymmetric synthesis to introduce chiral centers, it plays a role in the development of biologically active compounds, including antiviral and anti-inflammatory agents. Also utilized in the preparation of prodrugs due to the ester moiety, which can improve bioavailability.

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