1-(4-Bromobenzyl)-3-hydroxyazetidine

≥97%

Reagent Code: #171707
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CAS Number 1054483-33-8

science Other reagents with same CAS 1054483-33-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.11 g/mol
Formula C₁₀H₁₂BrNO
badge Registry Numbers
MDL Number MFCD11849010
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of receptor agonists and enzyme inhibitors. Its structure, featuring a hydroxy group and a 4-bromobenzyl substituent, facilitates easy modification to create derivatives for structure-activity relationship (SAR) studies. This supports the design of central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry for lead optimization in drug discovery programs targeting neurological disorders and inflammatory conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,010.00
inventory 1g
10-20 days ฿19,740.00
inventory 5g
10-20 days ฿64,180.00

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1-(4-Bromobenzyl)-3-hydroxyazetidine
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of receptor agonists and enzyme inhibitors. Its structure, featuring a hydroxy group and a 4-bromobenzyl substituent, facilitates easy modification to create derivatives for structure-activity relationship (SAR) studies. This supports the design of central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of receptor agonists and enzyme inhibitors. Its structure, featuring a hydroxy group and a 4-bromobenzyl substituent, facilitates easy modification to create derivatives for structure-activity relationship (SAR) studies. This supports the design of central nervous system agents due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry for lead optimization in drug discovery programs targeting neurological disorders and inflammatory conditions.

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