| Chemical Name: | (R)-2-Amino-3-(thiazol-5-yl)propanoic acid |
| CAS Number: | 321885-21-6 |
| Product Number: | AG00CNDN(AGN-PC-0WAI0P) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C6H8N2O2S |
| Molecular Weight: | 172.20492 |
The (R)-2-Amino-3-(thiazol-5-yl)propanoic acid, commonly known as $name$, serves as a crucial building block in chemical synthesis processes. This compound plays a pivotal role in the creation of various pharmaceuticals, agrochemicals, and specialized materials. Its unique structure containing a thiazole ring and an amino acid moiety makes it an invaluable component in the development of novel molecules with diverse functionalities.In chemical synthesis, $name$ is frequently used as a chiral auxiliary, enabling the construction of enantiomerically pure compounds. By harnessing its chirality, chemists can selectively control the stereochemistry of reactions, leading to the formation of specific enantiomers. This is particularly important in drug discovery and development, where the biological activity of a compound is often dictated by its stereochemistry.Additionally, (R)-2-Amino-3-(thiazol-5-yl)propanoic acid can serve as a precursor for the synthesis of complex molecules such as peptidomimetics and heterocyclic compounds. Its inclusion in synthetic pathways facilitates the formation of intricate chemical structures, allowing for the tailored design of compounds with desired properties.Overall, the versatile nature of $name$ makes it an indispensable tool in the field of chemical synthesis, enabling researchers to access a wide array of molecular structures with enhanced functionalities and applications.
![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)
O)Cc1cncs1](https://img.angenechemical.com/storage/c4d3/c4d30bfdcf94eb955f3893c4e7af17cb.png)