2-amino-4-chlorothiazole-5-carbaldehyde
95%
- Product Code: 135103
CAS:
76874-79-8
| Molecular Weight: | 162.60 g./mol | Molecular Formula: | C₄H₃ClN₂OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00204993 | |
| Melting Point: | Boiling Point: | 341.3±22.0 °C(Predicted) | |
| Density: | 1.658±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of thiazole-based antibiotics such as sulfathiazole and other sulfonamide drugs. It plays an important role in the development of active pharmaceutical ingredients (APIs) due to its reactive functional groups, which allow for easy modification and incorporation into larger drug molecules. Its structure supports the formation of heterocyclic compounds with antimicrobial and anti-inflammatory properties. Additionally, it is employed in the preparation of agrochemicals and dyes, where the aldehyde and amino groups facilitate coupling reactions and molecular elongation. Its versatility makes it valuable in research and industrial settings for developing bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,620.00 |
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| 5g | 10-20 days | ฿7,980.00 |
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| 10g | 10-20 days | ฿14,230.00 |
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| 25g | 10-20 days | ฿29,540.00 |
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2-amino-4-chlorothiazole-5-carbaldehyde
Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of thiazole-based antibiotics such as sulfathiazole and other sulfonamide drugs. It plays an important role in the development of active pharmaceutical ingredients (APIs) due to its reactive functional groups, which allow for easy modification and incorporation into larger drug molecules. Its structure supports the formation of heterocyclic compounds with antimicrobial and anti-inflammatory properties. Additionally, it is employed in the preparation of agrochemicals and dyes, where the aldehyde and amino groups facilitate coupling reactions and molecular elongation. Its versatility makes it valuable in research and industrial settings for developing bioactive compounds.
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