1-Bromo-2,3-bis(bromomethyl)benzene

95%

Reagent Code: #148792
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CAS Number 127168-82-5

science Other reagents with same CAS 127168-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.85 g/mol
Formula C₈H₇Br₃
badge Registry Numbers
MDL Number MFCD20483255
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its multiple bromomethyl groups allow for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it also serves in the development of polymers and specialty resins where controlled reactivity is required. Its structure enables the introduction of benzyl groups in various synthetic pathways, especially in the creation of ligands and functionalized aromatic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,280.00
inventory 250mg
10-20 days ฿4,560.00

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1-Bromo-2,3-bis(bromomethyl)benzene
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its multiple bromomethyl groups allow for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it also serves in the development of polymers and specialty resins where controlled reactivity is required. Its structure enables the introduction of benzyl groups in various synthetic pathw

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its multiple bromomethyl groups allow for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions to form carbon-carbon bonds, it also serves in the development of polymers and specialty resins where controlled reactivity is required. Its structure enables the introduction of benzyl groups in various synthetic pathways, especially in the creation of ligands and functionalized aromatic systems.

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