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
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
Appearance Yellow Solid
Purity (%) 91.5-100
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.500 10-20 days ฿17,080.00
+
-
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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