7-Amino-3-chloromethyl-3-cephem-4-carboxylic Acid Diphenylmethyl Ester Hydrochloride
95%
- Product Code: 96303
CAS:
79349-53-4
| Molecular Weight: | 451.37 g./mol | Molecular Formula: | C₂₁H₂₀Cl₂N₂O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191256 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in the synthesis of cephalosporin antibiotics, which are widely employed to treat bacterial infections. Its structure serves as a key intermediate in the production of advanced cephalosporin derivatives, enhancing their efficacy and spectrum of activity. The diphenylmethyl ester group protects the carboxylic acid functionality during chemical transformations, ensuring the stability and reactivity of the molecule. This compound is particularly valuable in pharmaceutical research and development, where it aids in the creation of novel antibiotics to combat resistant bacterial strains. Its role in the synthesis process is critical for achieving high-purity, biologically active end products.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to yellow powder to crystalline powder |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿15,970.00 |
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7-Amino-3-chloromethyl-3-cephem-4-carboxylic Acid Diphenylmethyl Ester Hydrochloride
This compound is primarily used in the synthesis of cephalosporin antibiotics, which are widely employed to treat bacterial infections. Its structure serves as a key intermediate in the production of advanced cephalosporin derivatives, enhancing their efficacy and spectrum of activity. The diphenylmethyl ester group protects the carboxylic acid functionality during chemical transformations, ensuring the stability and reactivity of the molecule. This compound is particularly valuable in pharmaceutical research and development, where it aids in the creation of novel antibiotics to combat resistant bacterial strains. Its role in the synthesis process is critical for achieving high-purity, biologically active end products.
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