1-tert-Butyl-3-ethylbenzene
98%
- Product Code: 114616
CAS:
14411-56-4
Molecular Weight: | 162.28 g./mol | Molecular Formula: | C₁₂H₁₈ |
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EC Number: | MDL Number: | MFCD00060845 | |
Melting Point: | Boiling Point: | 205 °C | |
Density: | 0.86 | Storage Condition: | Room temperature, sealed, dry |
Product Description:
1-tert-Butyl-3-ethylbenzene is primarily used in the field of organic synthesis as an intermediate for the production of more complex chemical compounds. Its structure makes it suitable for applications in the development of specialty chemicals, including fragrances and flavoring agents, where its unique aromatic properties can be leveraged. Additionally, it serves as a building block in the synthesis of polymers and resins, contributing to the creation of materials with specific physical and chemical properties. In the pharmaceutical industry, it may be utilized in the preparation of active pharmaceutical ingredients (APIs) or as a precursor in the synthesis of drug molecules. Its role in research and development is also notable, particularly in studies focusing on the behavior and reactivity of substituted benzene derivatives.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿5,310.00 |
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1-tert-Butyl-3-ethylbenzene
1-tert-Butyl-3-ethylbenzene is primarily used in the field of organic synthesis as an intermediate for the production of more complex chemical compounds. Its structure makes it suitable for applications in the development of specialty chemicals, including fragrances and flavoring agents, where its unique aromatic properties can be leveraged. Additionally, it serves as a building block in the synthesis of polymers and resins, contributing to the creation of materials with specific physical and chemical properties. In the pharmaceutical industry, it may be utilized in the preparation of active pharmaceutical ingredients (APIs) or as a precursor in the synthesis of drug molecules. Its role in research and development is also notable, particularly in studies focusing on the behavior and reactivity of substituted benzene derivatives.
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