2-(4-Bromobutyl)-1,3-dioxolane

96%

Reagent Code: #115759
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CAS Number 87227-41-6

science Other reagents with same CAS 87227-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.08 g/mol
Formula C₇H₁₃BrO₂
badge Registry Numbers
MDL Number MFCD02093454
inventory_2 Storage & Handling
Density 1.38g/mL
Storage 2-8°C, inert gas storage

description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a bromobutyl group attached to a dioxolane ring, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom serves as a reactive site for further functionalization through substitution reactions, enabling the creation of diverse compounds. Additionally, the dioxolane moiety can act as a protecting group for carbonyl functionalities in synthetic pathways, enhancing selectivity and yield in multi-step reactions. Its application is particularly significant in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals where precise molecular modifications are required.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,896.00
2-(4-Bromobutyl)-1,3-dioxolane
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This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a bromobutyl group attached to a dioxolane ring, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom serves as a reactive site for further functionalization through substitution reactions, enabling the creation of diverse compounds. Additionally, the dioxolane moiety can act as a p

This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a bromobutyl group attached to a dioxolane ring, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The bromine atom serves as a reactive site for further functionalization through substitution reactions, enabling the creation of diverse compounds. Additionally, the dioxolane moiety can act as a protecting group for carbonyl functionalities in synthetic pathways, enhancing selectivity and yield in multi-step reactions. Its application is particularly significant in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals where precise molecular modifications are required.

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