1-Bromo-4-(3-bromopropyl)benzene

95%

Reagent Code: #148411
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CAS Number 90562-10-0

science Other reagents with same CAS 90562-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.98 g/mol
Formula C₉H₁₀Br₂
badge Registry Numbers
MDL Number MFCD09744416
thermostat Physical Properties
Boiling Point 281.5±15.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its dual bromine functionality allows for sequential substitution reactions, enabling controlled chain extension or cross-linking in polymer chemistry. Commonly employed in the synthesis of liquid crystals and conjugated organic materials for electronic applications due to its ability to bridge aromatic and aliphatic segments. Also utilized in pharmaceutical research to construct complex molecular architectures through palladium-catalyzed coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,150.00
inventory 250mg
10-20 days ฿2,200.00

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1-Bromo-4-(3-bromopropyl)benzene
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Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its dual bromine functionality allows for sequential substitution reactions, enabling controlled chain extension or cross-linking in polymer chemistry. Commonly employed in the synthesis of liquid crystals and conjugated organic materials for electronic applications due to its ability to bridge aromatic and aliphatic segments. Also utilized in pharmaceutical research to construct co

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its dual bromine functionality allows for sequential substitution reactions, enabling controlled chain extension or cross-linking in polymer chemistry. Commonly employed in the synthesis of liquid crystals and conjugated organic materials for electronic applications due to its ability to bridge aromatic and aliphatic segments. Also utilized in pharmaceutical research to construct complex molecular architectures through palladium-catalyzed coupling reactions.

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