2-benzylidene-indan-1,3-dione

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Reagent Code: #142060
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CAS Number 5381-33-9

science Other reagents with same CAS 5381-33-9

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scatter_plot Molecular Information
Weight 234.25 g/mol
Formula C₁₆H₁₀O₂
badge Registry Numbers
MDL Number MFCD00156797
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the development of photochromic and electroactive materials. It serves in the preparation of functional dyes and pigments due to its conjugated structure and light-responsive properties. Applied in research for organic semiconductors and nonlinear optical materials. Also explored in medicinal chemistry for its potential bioactivity, including anti-inflammatory and anticancer properties, owing to its ability to interact with biological targets through π-π stacking and hydrogen bonding.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,950.00
inventory 250mg
10-20 days ฿9,720.00
inventory 1g
10-20 days ฿28,800.00

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2-benzylidene-indan-1,3-dione
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Used as a key intermediate in organic synthesis, particularly in the development of photochromic and electroactive materials. It serves in the preparation of functional dyes and pigments due to its conjugated structure and light-responsive properties. Applied in research for organic semiconductors and nonlinear optical materials. Also explored in medicinal chemistry for its potential bioactivity, including anti-inflammatory and anticancer properties, owing to its ability to interact with biological targe

Used as a key intermediate in organic synthesis, particularly in the development of photochromic and electroactive materials. It serves in the preparation of functional dyes and pigments due to its conjugated structure and light-responsive properties. Applied in research for organic semiconductors and nonlinear optical materials. Also explored in medicinal chemistry for its potential bioactivity, including anti-inflammatory and anticancer properties, owing to its ability to interact with biological targets through π-π stacking and hydrogen bonding.

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