2-Butyl-5-nitrobenzofuran
98%
- Product Code: 42233
CAS:
133238-87-6
Molecular Weight: | 219.24 g./mol | Molecular Formula: | C₁₂H₁₃NO₃ |
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EC Number: | MDL Number: | MFCD14525624 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceutical agents. Its structure is particularly valuable in the development of drugs targeting cardiovascular diseases, where it aids in the creation of compounds with vasodilatory properties. Additionally, it finds application in the synthesis of nitroaromatic compounds, which are essential in the manufacture of dyes and pigments. Its nitro group also makes it a candidate for research in the field of energetic materials, contributing to the development of propellants and explosives. In laboratory settings, it is utilized for studying reaction mechanisms involving nitroaromatics, providing insights into their behavior under different chemical conditions.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White to Yellow to Brown solid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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10.000 | 10-20 days | ฿3,880.00 |
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50.000 | 10-20 days | ฿15,760.00 |
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2-Butyl-5-nitrobenzofuran
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceutical agents. Its structure is particularly valuable in the development of drugs targeting cardiovascular diseases, where it aids in the creation of compounds with vasodilatory properties. Additionally, it finds application in the synthesis of nitroaromatic compounds, which are essential in the manufacture of dyes and pigments. Its nitro group also makes it a candidate for research in the field of energetic materials, contributing to the development of propellants and explosives. In laboratory settings, it is utilized for studying reaction mechanisms involving nitroaromatics, providing insights into their behavior under different chemical conditions.
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