(2-Chloro-5-iodophenyl)(4-ethoxyphenyl)methanone
97%
- Product Code: 113092
CAS:
1103738-26-6
Molecular Weight: | 386.61 g./mol | Molecular Formula: | C₁₅H₁₂ClIO₂ |
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EC Number: | MDL Number: | MFCD18642360 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring both chloro and iodo substituents, makes it a versatile building block for constructing complex organic molecules. Researchers often employ it in cross-coupling reactions, such as Suzuki or Sonogashira reactions, to create novel compounds for drug discovery. Additionally, its methanone core can be modified to explore new chemical entities with potential anti-inflammatory, antimicrobial, or anticancer properties. Its role in medicinal chemistry highlights its importance in advancing the development of new pharmaceuticals.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿747.00 |
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1.000 | 10-20 days | ฿1,485.00 |
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(2-Chloro-5-iodophenyl)(4-ethoxyphenyl)methanone
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring both chloro and iodo substituents, makes it a versatile building block for constructing complex organic molecules. Researchers often employ it in cross-coupling reactions, such as Suzuki or Sonogashira reactions, to create novel compounds for drug discovery. Additionally, its methanone core can be modified to explore new chemical entities with potential anti-inflammatory, antimicrobial, or anticancer properties. Its role in medicinal chemistry highlights its importance in advancing the development of new pharmaceuticals.
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