2-bromothiazole-5-carbaldehyde
98%
- Product Code: 143858
CAS:
464192-28-7
| Molecular Weight: | 192.04 g./mol | Molecular Formula: | C₄H₂BrNOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03788567 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing biologically active molecules. Commonly employed in the development of fungicides and insecticides due to the thiazole ring’s inherent bioactivity. Also utilized in the preparation of fluorescent dyes and optical brighteners, where it contributes to electron-withdrawing properties that enhance photostability. In medicinal chemistry, it serves as a building block for kinase inhibitors and antimicrobial agents. Its aldehyde group enables easy derivatization through condensation reactions, facilitating rapid library synthesis in drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5-100 |
| Appearance | Brown powder |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | $9.62 |
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| 5g | 10-20 days | $69.54 |
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2-bromothiazole-5-carbaldehyde
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing biologically active molecules. Commonly employed in the development of fungicides and insecticides due to the thiazole ring’s inherent bioactivity. Also utilized in the preparation of fluorescent dyes and optical brighteners, where it contributes to electron-withdrawing properties that enhance photostability. In medicinal chemistry, it serves as a building block for kinase inhibitors and antimicrobial agents. Its aldehyde group enables easy derivatization through condensation reactions, facilitating rapid library synthesis in drug discovery.
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