1-Oxo-2,3-dihydro-1H-inden-4-yl benzoate

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Reagent Code: #222421
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CAS Number 59725-61-0

science Other reagents with same CAS 59725-61-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.269 g/mol
Formula C₁₆H₁₂O₃
thermostat Physical Properties
Melting Point 78-82 °C(lit.)
Boiling Point 470 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its structure supports use in esterification and carbonyl-related reactions, making it valuable in creating biologically active compounds. Commonly employed in research settings for designing molecules with potential anti-inflammatory or analgesic properties. Also utilized in the preparation of specialty polymers and functional materials due to its aromatic and reactive functional group arrangement.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,500.00
inventory 1g
10-20 days ฿14,810.00
inventory 5g
10-20 days ฿56,130.00

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1-Oxo-2,3-dihydro-1H-inden-4-yl benzoate
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its structure supports use in esterification and carbonyl-related reactions, making it valuable in creating biologically active compounds. Commonly employed in research settings for designing molecules with potential anti-inflammatory or analgesic properties. Also utilized in the preparation of specialty polymers and functional materials due to its aromatic and reactive functional group ar

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its structure supports use in esterification and carbonyl-related reactions, making it valuable in creating biologically active compounds. Commonly employed in research settings for designing molecules with potential anti-inflammatory or analgesic properties. Also utilized in the preparation of specialty polymers and functional materials due to its aromatic and reactive functional group arrangement.

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