m-Carborane-1,7-dicarboxylic Acid

98%

Reagent Code: #114231
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CAS Number 50571-15-8

science Other reagents with same CAS 50571-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.24 g/mol
Formula C₄H₁₂B₁₀O₄
badge Registry Numbers
MDL Number MFCD00157045
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

m-Carborane-1,7-dicarboxylic acid finds significant applications in the field of medicinal chemistry and materials science due to its unique structural and chemical properties. In medicinal chemistry, it is utilized as a building block for the development of boron neutron capture therapy (BNCT) agents. Its carborane core allows for efficient boron delivery to cancer cells, enabling targeted treatment with minimal damage to surrounding healthy tissues. In materials science, this compound is employed in the synthesis of advanced polymers and coatings. Its thermal stability and resistance to harsh chemical environments make it suitable for creating high-performance materials used in extreme conditions. Additionally, it serves as a precursor for the development of novel organic-inorganic hybrid materials, which are explored for their potential in electronics, catalysis, and nanotechnology. The dicarboxylic acid groups further enable its functionalization, allowing for tailored modifications to meet specific application requirements.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿2,592.00

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m-Carborane-1,7-dicarboxylic Acid
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m-Carborane-1,7-dicarboxylic acid finds significant applications in the field of medicinal chemistry and materials science due to its unique structural and chemical properties. In medicinal chemistry, it is utilized as a building block for the development of boron neutron capture therapy (BNCT) agents. Its carborane core allows for efficient boron delivery to cancer cells, enabling targeted treatment with minimal damage to surrounding healthy tissues. In materials science, this compound is employed in the synthesis of advanced polymers and coatings. Its thermal stability and resistance to harsh chemical environments make it suitable for creating high-performance materials used in extreme conditions. Additionally, it serves as a precursor for the development of novel organic-inorganic hybrid materials, which are explored for their potential in electronics, catalysis, and nanotechnology. The dicarboxylic acid groups further enable its functionalization, allowing for tailored modifications to meet specific application requirements.
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