trans-2-(2-fluoro-5-nitrophenyl)cyclopropane-1-carboxylic acid
92%
- Product Code: 106608
CAS:
2227755-27-1
Molecular Weight: | 225.18 g./mol | Molecular Formula: | C₁₀H₈FNO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a cyclopropane ring and a nitro group, makes it valuable for designing molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in drug discovery programs to explore its efficacy in modulating biological pathways. Additionally, its unique chemical properties allow for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.
Product Specification:
Test | Specification |
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Appearance | Yellow Solid |
Purity (%) | 91.5-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.500 | 10-20 days | ฿17,080.00 |
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1.000 | 10-20 days | ฿25,000.00 |
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5.000 | 10-20 days | ฿84,000.00 |
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trans-2-(2-fluoro-5-nitrophenyl)cyclopropane-1-carboxylic acid
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a cyclopropane ring and a nitro group, makes it valuable for designing molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in drug discovery programs to explore its efficacy in modulating biological pathways. Additionally, its unique chemical properties allow for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.
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