1,2-Dihydronaphthalene

98%

Reagent Code: #174019
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CAS Number 447-53-0

science Other reagents with same CAS 447-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.19 g/mol
Formula C₁₀H₁₀
badge Registry Numbers
MDL Number MFCD00001672
thermostat Physical Properties
Melting Point -8°C(lit.)
Boiling Point 207°C
inventory_2 Storage & Handling
Density 1g/mL
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for more complex aromatic compounds due to its reactive double bond within the fused ring system. Commonly employed in hydrogenation and oxidation reactions to yield tetralin or naphthalene derivatives. Also utilized in research settings for studying pericyclic reactions and cyclization processes. Its ability to act as a diene in Diels-Alder reactions makes it valuable in creating polycyclic structures found in natural products and advanced materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿1,320.00
inventory 25g
10-20 days ฿5,390.00
inventory 100g
10-20 days ฿21,000.00
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1,2-Dihydronaphthalene
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for more complex aromatic compounds due to its reactive double bond within the fused ring system. Commonly employed in hydrogenation and oxidation reactions to yield tetralin or naphthalene derivatives. Also utilized in research settings for studying pericyclic reactions and cyclization processes. Its ability to act as a diene in Diels-Alder reactions m

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for more complex aromatic compounds due to its reactive double bond within the fused ring system. Commonly employed in hydrogenation and oxidation reactions to yield tetralin or naphthalene derivatives. Also utilized in research settings for studying pericyclic reactions and cyclization processes. Its ability to act as a diene in Diels-Alder reactions makes it valuable in creating polycyclic structures found in natural products and advanced materials.

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