2,7-Diiodonaphthalene

97%

Reagent Code: #178687
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CAS Number 58556-77-7

science Other reagents with same CAS 58556-77-7

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inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated organic materials for optoelectronic devices. It serves as a building block in the formation of naphthalene-based polymers and small molecules used in organic semiconductors, OLEDs, and field-effect transistors. The iodine atoms enable further functionalization through cross-coupling reactions like Suzuki or Heck couplings, allowing precise extension of π-conjugated systems. Its rigid aromatic structure contributes to thermal stability and favorable charge transport properties in thin-film devices. Also employed in the synthesis of fluorescent dyes and probes where halogenated naphthalene cores enhance photophysical characteristics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,210.00
inventory 250mg
10-20 days ฿6,970.00
inventory 1g
10-20 days ฿22,480.00

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2,7-Diiodonaphthalene
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Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated organic materials for optoelectronic devices. It serves as a building block in the formation of naphthalene-based polymers and small molecules used in organic semiconductors, OLEDs, and field-effect transistors. The iodine atoms enable further functionalization through cross-coupling reactions like Suzuki or Heck couplings, allowing precise extension of π-conjugated systems. Its rigid aromatic structure contrib

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated organic materials for optoelectronic devices. It serves as a building block in the formation of naphthalene-based polymers and small molecules used in organic semiconductors, OLEDs, and field-effect transistors. The iodine atoms enable further functionalization through cross-coupling reactions like Suzuki or Heck couplings, allowing precise extension of π-conjugated systems. Its rigid aromatic structure contributes to thermal stability and favorable charge transport properties in thin-film devices. Also employed in the synthesis of fluorescent dyes and probes where halogenated naphthalene cores enhance photophysical characteristics.

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