Bromoiodomethane
97%
- Product Code: 122850
CAS:
557-68-6
Molecular Weight: | 220.84 g./mol | Molecular Formula: | CH₂BrI |
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EC Number: | MDL Number: | MFCD00041452 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
Bromoiodomethane is primarily used in organic synthesis as a reagent for introducing methylene groups into various compounds. It is particularly valuable in the preparation of cyclopropane derivatives through the Simmons-Smith reaction, where it acts as a carbene precursor. Additionally, it serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, enabling the formation of complex molecular structures. Its dual halogen functionality allows for selective reactivity in cross-coupling reactions, making it useful in the development of fine chemicals. Bromoiodomethane is also employed in research settings for studying reaction mechanisms and exploring new synthetic pathways.
Product Specification:
Test | Specification |
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Appearance | Colorless Liquid |
Purity (%) | 96.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | Ft8,511.55 |
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25.000 | 10-20 days | Ft33,830.70 |
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100.000 | 10-20 days | Ft127,457.70 |
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Bromoiodomethane
Bromoiodomethane is primarily used in organic synthesis as a reagent for introducing methylene groups into various compounds. It is particularly valuable in the preparation of cyclopropane derivatives through the Simmons-Smith reaction, where it acts as a carbene precursor. Additionally, it serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, enabling the formation of complex molecular structures. Its dual halogen functionality allows for selective reactivity in cross-coupling reactions, making it useful in the development of fine chemicals. Bromoiodomethane is also employed in research settings for studying reaction mechanisms and exploring new synthetic pathways.
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