3-(Phenylethynyl)aniline

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Reagent Code: #227062
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CAS Number 51624-44-3

science Other reagents with same CAS 51624-44-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.24 g/mol
Formula C₁₄H₁₁N
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MDL Number MFCD08701708
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and optoelectronic compounds. Its structure supports extended π-conjugation, making it valuable in organic semiconductors and light-emitting diodes (OLEDs). Also employed in the preparation of specialty dyes and fluorescent probes due to its stable aromatic amine functionality and ability to undergo selective derivatization. Additionally, it serves as a building block in pharmaceutical research for constructing bioactive molecules with tailored electronic and structural properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,810.00
inventory 250mg
10-20 days ฿8,790.00
inventory 1g
10-20 days ฿29,040.00

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3-(Phenylethynyl)aniline
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Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and optoelectronic compounds. Its structure supports extended π-conjugation, making it valuable in organic semiconductors and light-emitting diodes (OLEDs). Also employed in the preparation of specialty dyes and fluorescent probes due to its stable aromatic amine functionality and ability to undergo selective derivatization. Additionally, it serves as a building block in pharm

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and optoelectronic compounds. Its structure supports extended π-conjugation, making it valuable in organic semiconductors and light-emitting diodes (OLEDs). Also employed in the preparation of specialty dyes and fluorescent probes due to its stable aromatic amine functionality and ability to undergo selective derivatization. Additionally, it serves as a building block in pharmaceutical research for constructing bioactive molecules with tailored electronic and structural properties.

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