tert-Butyl ((6-chloropyrazin-2-yl)methyl)carbamate
97%
- Product Code: 36086
CAS:
1187222-00-9
| Molecular Weight: | 243.6901 g./mol | Molecular Formula: | C₁₀H₁₄ClN₃O₂ |
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| EC Number: | MDL Number: | MFCD20327987 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl ((6-chloropyrazin-2-yl)methyl)carbamate is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of drugs targeting specific enzymes or receptors. Its structure, featuring a chloropyrazine moiety, makes it valuable for constructing complex molecules with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, it is utilized in the preparation of peptide-based compounds, where the tert-butyl carbamate group acts as a protecting group for amines during multi-step synthetic processes. This chemical is also explored in agrochemical research for designing novel pesticides or herbicides due to its reactivity and structural versatility.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $327.72 |
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tert-Butyl ((6-chloropyrazin-2-yl)methyl)carbamate
tert-Butyl ((6-chloropyrazin-2-yl)methyl)carbamate is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of drugs targeting specific enzymes or receptors. Its structure, featuring a chloropyrazine moiety, makes it valuable for constructing complex molecules with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, it is utilized in the preparation of peptide-based compounds, where the tert-butyl carbamate group acts as a protecting group for amines during multi-step synthetic processes. This chemical is also explored in agrochemical research for designing novel pesticides or herbicides due to its reactivity and structural versatility.
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