4-Chloro-3-iodobenzotrifluoride
98%
- Product Code: 66318
CAS:
672-57-1
Molecular Weight: | 306.45 g./mol | Molecular Formula: | C₇H₃ClF₃I |
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Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
4-Chloro-3-iodobenzotrifluoride is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents on a benzotrifluoride core, makes it particularly valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the creation of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the compound’s stability and influences the electronic properties of the resulting products, making it useful in the design of bioactive molecules. Additionally, it serves as an intermediate in the synthesis of liquid crystals and other specialty chemicals used in electronics and optics. Its halogenated structure also allows for further functionalization, enabling researchers to tailor its properties for specific applications in medicinal chemistry and material science.
Product Specification:
Test | Specification |
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Purity | 97.5-100 |
Melting point | 28-32 |
REFRACTIVE INDEX N20D | 1.535-1.539 |
Appearance | Colorless to yellow Liquid or Low melting crystalline solid |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $15.03 |
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25.000 | 10-20 days | $47.90 |
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100.000 | 10-20 days | $182.22 |
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500.000 | 10-20 days | $648.10 |
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4-Chloro-3-iodobenzotrifluoride
4-Chloro-3-iodobenzotrifluoride is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents on a benzotrifluoride core, makes it particularly valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the creation of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the compound’s stability and influences the electronic properties of the resulting products, making it useful in the design of bioactive molecules. Additionally, it serves as an intermediate in the synthesis of liquid crystals and other specialty chemicals used in electronics and optics. Its halogenated structure also allows for further functionalization, enabling researchers to tailor its properties for specific applications in medicinal chemistry and material science.
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