1-(Benzyloxy)-4-(bromomethyl)benzene

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Reagent Code: #119636
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CAS Number 5544-60-5

science Other reagents with same CAS 5544-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.16 g/mol
Formula C₁₄H₁₃BrO
thermostat Physical Properties
Boiling Point 366°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in pharmaceutical research and development. The benzyloxy group offers protective functionality for hydroxyl groups during synthetic processes, while the bromomethyl group serves as a reactive site for further chemical modifications, such as nucleophilic substitution reactions. Its applications extend to the synthesis of various bioactive compounds, including potential drug candidates, where precise control over molecular structure is crucial. Additionally, it can be used in material science for the development of specialized polymers or coatings, leveraging its reactive bromomethyl group for cross-linking or functionalization purposes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,900.00
inventory 100mg
10-20 days ฿4,590.00

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1-(Benzyloxy)-4-(bromomethyl)benzene
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in pharmaceutical research and development. The benzyloxy group offers protective functionality for hydroxyl groups during synthetic processes, while the bromomethyl group serves as a reactive site for further chemical modifications, such as nucleophilic substitution reactions. Its applications extend to the synthesis of various bioactive co

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of more complex molecules, particularly in pharmaceutical research and development. The benzyloxy group offers protective functionality for hydroxyl groups during synthetic processes, while the bromomethyl group serves as a reactive site for further chemical modifications, such as nucleophilic substitution reactions. Its applications extend to the synthesis of various bioactive compounds, including potential drug candidates, where precise control over molecular structure is crucial. Additionally, it can be used in material science for the development of specialized polymers or coatings, leveraging its reactive bromomethyl group for cross-linking or functionalization purposes.

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