Acenaphthylene

95%

Reagent Code: #134799
label
Alias acetoethylene;naphthalene, naphthalene, 1,8-ethylenenaphthalene
fingerprint
CAS Number 208-96-8

science Other reagents with same CAS 208-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.19 g/mol
Formula C₁₂H₈
badge Registry Numbers
EC Number 203-806-2
MDL Number MFCD00003806
thermostat Physical Properties
Melting Point 78-82 °C(lit.)
Boiling Point 280 °C(lit.)
inventory_2 Storage & Handling
Density 0.899 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used in organic synthesis, particularly in the development of polycyclic aromatic hydrocarbon (PAH) frameworks. Serves as a building block for dyes, pharmaceuticals, and functional materials. Employed in research to create conjugated systems for optoelectronic applications such as organic semiconductors and fluorescent probes. Also utilized in the study of reaction mechanisms involving strained olefins due to its unique bicyclic structure with a reactive double bond.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿850.00
inventory 25g
10-20 days ฿3,490.00
inventory 100g
10-20 days ฿13,380.00

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Acenaphthylene
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Used in organic synthesis, particularly in the development of polycyclic aromatic hydrocarbon (PAH) frameworks. Serves as a building block for dyes, pharmaceuticals, and functional materials. Employed in research to create conjugated systems for optoelectronic applications such as organic semiconductors and fluorescent probes. Also utilized in the study of reaction mechanisms involving strained olefins due to its unique bicyclic structure with a reactive double bond.

Used in organic synthesis, particularly in the development of polycyclic aromatic hydrocarbon (PAH) frameworks. Serves as a building block for dyes, pharmaceuticals, and functional materials. Employed in research to create conjugated systems for optoelectronic applications such as organic semiconductors and fluorescent probes. Also utilized in the study of reaction mechanisms involving strained olefins due to its unique bicyclic structure with a reactive double bond.

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