1,8-Dibromo-3-(methoxymethoxy)naphthalene

98%

Reagent Code: #180012
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CAS Number 2648221-47-8

science Other reagents with same CAS 2648221-47-8

blur_circular Chemical Specifications

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Weight 346.01 g/mol
Formula C₁₂H₁₀Br₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized naphthalene derivatives for optoelectronic materials. It serves in the construction of conjugated systems for organic semiconductors and fluorescent dyes. The bromine groups allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the assembly of complex aromatic structures. The methoxymethoxy group acts as a protecting group for phenolic hydroxyls, making it valuable in multi-step synthesis where selective deprotection is required. Commonly applied in the development of organic light-emitting diodes (OLEDs) and sensors.

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inventory 100mg
10-20 days ฿15,050.00

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1,8-Dibromo-3-(methoxymethoxy)naphthalene
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Used as an intermediate in organic synthesis, particularly in the preparation of functionalized naphthalene derivatives for optoelectronic materials. It serves in the construction of conjugated systems for organic semiconductors and fluorescent dyes. The bromine groups allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the assembly of complex aromatic structures. The methoxymethoxy group acts as a protecting group for phenolic hydroxyls, making it

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized naphthalene derivatives for optoelectronic materials. It serves in the construction of conjugated systems for organic semiconductors and fluorescent dyes. The bromine groups allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the assembly of complex aromatic structures. The methoxymethoxy group acts as a protecting group for phenolic hydroxyls, making it valuable in multi-step synthesis where selective deprotection is required. Commonly applied in the development of organic light-emitting diodes (OLEDs) and sensors.

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