4,4,4-Trifluoro-1-(4-methoxyphenyl)-1,3-butanedione
≥98%
- Product Code: 68030
CAS:
15191-68-1
Molecular Weight: | 246.19 g./mol | Molecular Formula: | C₁₁H₉F₃O₃ |
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EC Number: | MDL Number: | MFCD03238723 | |
Melting Point: | 56-60°C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, including those with anti-inflammatory and antimicrobial properties. Its unique structure allows it to participate in reactions that form heterocyclic compounds, which are often the backbone of many active pharmaceutical ingredients. Additionally, it is used in material science for the development of advanced materials with specific optical or electronic properties. In research, it is employed as a reagent in organic synthesis to study reaction mechanisms and develop new chemical processes. Its trifluoromethyl group enhances the stability and reactivity of the compounds it forms, making it valuable in high-performance applications.
Product Specification:
Test | Specification |
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APPEARANCE | White to Pale yellow Crystal or Powder |
PURITY | 98-100 |
MELTING POINT | 56.0-60.0 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿1,170.00 |
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1.000 | 10-20 days | ฿4,610.00 |
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5.000 | 10-20 days | ฿18,170.00 |
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4,4,4-Trifluoro-1-(4-methoxyphenyl)-1,3-butanedione
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, including those with anti-inflammatory and antimicrobial properties. Its unique structure allows it to participate in reactions that form heterocyclic compounds, which are often the backbone of many active pharmaceutical ingredients. Additionally, it is used in material science for the development of advanced materials with specific optical or electronic properties. In research, it is employed as a reagent in organic synthesis to study reaction mechanisms and develop new chemical processes. Its trifluoromethyl group enhances the stability and reactivity of the compounds it forms, making it valuable in high-performance applications.
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