3,5-Dibenzyloxybenzyl Bromide

98%

Reagent Code: #94513
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CAS Number 24131-32-6

science Other reagents with same CAS 24131-32-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.29 g/mol
Formula C₂₁H₁₉BrO₂
badge Registry Numbers
MDL Number MFCD02093444
thermostat Physical Properties
Melting Point 85.0-89.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It is employed in the development of compounds with potential therapeutic properties, such as anticancer or antimicrobial agents. The benzyloxy groups provide protection for hydroxyl functionalities during multi-step reactions, allowing selective transformations. Additionally, it serves as a building block in the synthesis of dendrimers and other polymeric materials, contributing to advancements in material science and drug delivery systems.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,690.00

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3,5-Dibenzyloxybenzyl Bromide
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Used in organic synthesis as an intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It is employed in the development of compounds with potential therapeutic properties, such as anticancer or antimicrobial agents. The benzyloxy groups provide protection for hydroxyl functionalities during multi-step reactions, allowing selective transformations. Additionally, it serves as a building block in the synthesis of dendrimers and other polymeric materials, contributin

Used in organic synthesis as an intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It is employed in the development of compounds with potential therapeutic properties, such as anticancer or antimicrobial agents. The benzyloxy groups provide protection for hydroxyl functionalities during multi-step reactions, allowing selective transformations. Additionally, it serves as a building block in the synthesis of dendrimers and other polymeric materials, contributing to advancements in material science and drug delivery systems.

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