| Chemical Name: | Amikacin sulfate salt |
| CAS Number: | 149022-22-0 |
| Product Number: | AG001LCO(AGN-PC-0Q2P45) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C22H45N5O17S |
| Molecular Weight: | 683.6810 |
O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1→4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine sulfate is a complex compound that finds crucial applications in chemical synthesis. This compound serves as a versatile building block in the synthesis of various glycoconjugates and glycopeptides due to its unique structure and functional groups.The α-D-glucopyranosyl and α-D-glycopyranosyl moieties present in the compound allow for selective glycosidic bond formation, enabling the creation of complex carbohydrate structures. Additionally, the amino and hydroxy functional groups provide sites for further chemical modification, allowing for the introduction of different chemical moieties to tailor the properties of the final product.With its intricate molecular architecture and multiple reactive sites, this compound plays a significant role in the design and synthesis of carbohydrate-based molecules with diverse applications in medicinal chemistry, bioconjugation, and materials science.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
N[C@@H]1C[C@H](N)[C@H]([C@@H]([C@H]1O[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)N)O)O)O[C@H]1O[C@H](CN)[C@H]([C@@H]([C@H]1O)O)O)O](https://img.angenechemical.com/storage/5b71/5b71902eb8b5cf53f8bae729196b693c.png)