(R)-2-(bromomethyl)-2,3-dihydrobenzo[b][1,4]dioxine

≥95%

Reagent Code: #37516
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CAS Number 1142953-55-6

science Other reagents with same CAS 1142953-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula C₉H₉BrO₂
thermostat Physical Properties
Boiling Point 288.3±19.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.501±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmacologically active molecules. Its structure, featuring a bromomethyl group attached to a 2,3-dihydrobenzo[b][1,4]dioxine ring with (R)-configuration, makes it a valuable chiral building block in the development of enantiomerically pure compounds, particularly in asymmetric synthesis. It is often employed in the synthesis of ligands and catalysts used in enantioselective reactions, which are crucial in producing drugs with high stereochemical purity. Additionally, it finds application in the creation of complex heterocyclic compounds that are explored for their potential biological activities, such as antimicrobial, anticancer, or central nervous system-targeting agents. Its reactivity allows for further functionalization, enabling the construction of diverse molecular frameworks in medicinal chemistry research.

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inventory 1g
10-20 days ฿48,393.00

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(R)-2-(bromomethyl)-2,3-dihydrobenzo[b][1,4]dioxine
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmacologically active molecules. Its structure, featuring a bromomethyl group attached to a 2,3-dihydrobenzo[b][1,4]dioxine ring with (R)-configuration, makes it a valuable chiral building block in the development of enantiomerically pure compounds, particularly in asymmetric synthesis. It is often employed in the synthesis of ligands and catalysts used in enantioselective reactions, which are

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmacologically active molecules. Its structure, featuring a bromomethyl group attached to a 2,3-dihydrobenzo[b][1,4]dioxine ring with (R)-configuration, makes it a valuable chiral building block in the development of enantiomerically pure compounds, particularly in asymmetric synthesis. It is often employed in the synthesis of ligands and catalysts used in enantioselective reactions, which are crucial in producing drugs with high stereochemical purity. Additionally, it finds application in the creation of complex heterocyclic compounds that are explored for their potential biological activities, such as antimicrobial, anticancer, or central nervous system-targeting agents. Its reactivity allows for further functionalization, enabling the construction of diverse molecular frameworks in medicinal chemistry research.

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