1-Bromo-2-(chloromethyl)benzene

≥98%(GC)

Reagent Code: #154797
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CAS Number 578-51-8

science Other reagents with same CAS 578-51-8

blur_circular Chemical Specifications

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Weight 205.48 g/mol
Formula C₇H₆BrCl
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing benzyl or substituted benzyl groups in various reactions. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) through nucleophilic substitution reactions. Also utilized in the preparation of ligands for catalysts and in the development of functionalized polymers. Its dual halogen functionality allows for selective and sequential reactions, making it valuable in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,750.00
inventory 25g
10-20 days ฿15,800.00

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1-Bromo-2-(chloromethyl)benzene
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing benzyl or substituted benzyl groups in various reactions. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) through nucleophilic substitution reactions. Also utilized in the preparation of ligands for catalysts and in the development of functionalized polymers. Its dual halogen functionality allows for selective and s

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing benzyl or substituted benzyl groups in various reactions. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) through nucleophilic substitution reactions. Also utilized in the preparation of ligands for catalysts and in the development of functionalized polymers. Its dual halogen functionality allows for selective and sequential reactions, making it valuable in multi-step synthetic routes.

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