5-Bromo-4-methyl-2,3-dihydro-1H-inden-1-one

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Reagent Code: #146604
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CAS Number 903557-48-2

science Other reagents with same CAS 903557-48-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.08 g/mol
Formula C₁₀H₉BrO
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with potential antidepressant, anxiolytic, and anticonvulsant properties. Commonly employed in organic synthesis for constructing complex indane-based frameworks found in bioactive molecules. Also utilized in research settings for structure-activity relationship (SAR) studies due to its halogenated aromatic core, which allows further functionalization via cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,030.00
inventory 100mg
10-20 days ฿7,290.00
inventory 250mg
10-20 days ฿12,220.00
inventory 1g
10-20 days ฿36,410.00

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5-Bromo-4-methyl-2,3-dihydro-1H-inden-1-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with potential antidepressant, anxiolytic, and anticonvulsant properties. Commonly employed in organic synthesis for constructing complex indane-based frameworks found in bioactive molecules. Also utilized in research settings for structure-activity relationship (SAR) studies due to its halogenated aromatic core, wh

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with potential antidepressant, anxiolytic, and anticonvulsant properties. Commonly employed in organic synthesis for constructing complex indane-based frameworks found in bioactive molecules. Also utilized in research settings for structure-activity relationship (SAR) studies due to its halogenated aromatic core, which allows further functionalization via cross-coupling reactions.

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