1-(anthracen-9-yl)-N-methylmethanamine

≥95%

Reagent Code: #218007
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CAS Number 73356-19-1

science Other reagents with same CAS 73356-19-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221 g/mol
Formula C₁₆H₁₅N
thermostat Physical Properties
Melting Point 57-59℃
Boiling Point 389℃
inventory_2 Storage & Handling
Density 1.11g/cm3
Storage 2-8°C

description Product Description

Used as a fluorescent probe in biochemical and analytical applications due to its strong anthracene-based fluorescence. Its amine functionality allows for chemical modification, making it useful in the synthesis of larger conjugated systems for optoelectronic devices such as organic light-emitting diodes (OLEDs). Also employed in the study of energy transfer processes and as a building block in supramolecular chemistry. Its planar anthracene moiety enables π-stacking interactions, beneficial in sensor design and molecular recognition studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿900.00
inventory 1g
10-20 days ฿2,530.00
inventory 5g
10-20 days ฿9,560.00
inventory 25g
10-20 days ฿40,970.00

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1-(anthracen-9-yl)-N-methylmethanamine
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Used as a fluorescent probe in biochemical and analytical applications due to its strong anthracene-based fluorescence. Its amine functionality allows for chemical modification, making it useful in the synthesis of larger conjugated systems for optoelectronic devices such as organic light-emitting diodes (OLEDs). Also employed in the study of energy transfer processes and as a building block in supramolecular chemistry. Its planar anthracene moiety enables π-stacking interactions, beneficial in sensor de

Used as a fluorescent probe in biochemical and analytical applications due to its strong anthracene-based fluorescence. Its amine functionality allows for chemical modification, making it useful in the synthesis of larger conjugated systems for optoelectronic devices such as organic light-emitting diodes (OLEDs). Also employed in the study of energy transfer processes and as a building block in supramolecular chemistry. Its planar anthracene moiety enables π-stacking interactions, beneficial in sensor design and molecular recognition studies.

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