Imidodicarbonic acid, (2-bromo-4-fluoro-6-nitrophenyl)-, bis(1,1-dimethylethyl) ester
98%
- Product Code: 123601
CAS:
880384-52-1
| Molecular Weight: | 435.24 g./mol | Molecular Formula: | C₁₆H₂₀BrFN₂O₆ |
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| EC Number: | MDL Number: | MFCD29472568 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as a specialized reagent for protecting and modifying functional groups, particularly in the development of complex molecules. Its unique structure allows it to act as a protective group for amines or other reactive sites during multi-step chemical reactions, ensuring selective transformations without unwanted side reactions. It is particularly valuable in pharmaceutical research, where it aids in the synthesis of drug intermediates or active pharmaceutical ingredients (APIs) with specific structural requirements. Additionally, its bromo, fluoro, and nitro substituents make it useful in the preparation of compounds for materials science, such as advanced polymers or agrochemicals, where these functional groups can influence reactivity and properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,067.00 |
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| 1.000 | 10-20 days | ฿10,143.00 |
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Imidodicarbonic acid, (2-bromo-4-fluoro-6-nitrophenyl)-, bis(1,1-dimethylethyl) ester
This chemical is primarily used in organic synthesis as a specialized reagent for protecting and modifying functional groups, particularly in the development of complex molecules. Its unique structure allows it to act as a protective group for amines or other reactive sites during multi-step chemical reactions, ensuring selective transformations without unwanted side reactions. It is particularly valuable in pharmaceutical research, where it aids in the synthesis of drug intermediates or active pharmaceutical ingredients (APIs) with specific structural requirements. Additionally, its bromo, fluoro, and nitro substituents make it useful in the preparation of compounds for materials science, such as advanced polymers or agrochemicals, where these functional groups can influence reactivity and properties.
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