Ethyl 2-(2-aminothiazol-4-yl)glyoxylate
98%
- Product Code: 182169
Alias:
Aminothiazole ethyl glycoloxylate; 2-(2-aminothiazole-4-yl)glyoxylate; 2-amino-4-thiazole ethyl glycoloxylate; ethyl 2-(2-aminothiazole-4-yl)glyoxylate; 2-(2-amino-4-thiazole)-2-oxoacetate
CAS:
64987-08-2
| Molecular Weight: | 200.22 g./mol | Molecular Formula: | C₇H₈N₂O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 150-152 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used as a key intermediate in the synthesis of β-lactam antibiotics, particularly cephalosporins. It plays a critical role in constructing the core structure of these antibiotics by enabling the introduction of the aminothiazole ring, which enhances antimicrobial activity and improves pharmacokinetic properties. Its reactivity allows for efficient coupling with various side chains, making it valuable in pharmaceutical research and development for creating semi-synthetic antibiotics. Commonly employed in multi-step organic syntheses where selective functional group transformations are required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25g | 10-20 days | ฿1,850.00 |
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| 100g | 10-20 days | ฿6,800.00 |
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| 500g | 10-20 days | ฿30,000.00 |
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Ethyl 2-(2-aminothiazol-4-yl)glyoxylate
Widely used as a key intermediate in the synthesis of β-lactam antibiotics, particularly cephalosporins. It plays a critical role in constructing the core structure of these antibiotics by enabling the introduction of the aminothiazole ring, which enhances antimicrobial activity and improves pharmacokinetic properties. Its reactivity allows for efficient coupling with various side chains, making it valuable in pharmaceutical research and development for creating semi-synthetic antibiotics. Commonly employed in multi-step organic syntheses where selective functional group transformations are required.
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