(4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid CAS: 143527-70-2
Catalog Number | XD94109 |
Product Name | (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid |
CAS | 143527-70-2 |
Molecular Formula | C17H23NO5 |
Molecular Weight | 321.37 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
The chemical compound (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid, also known as (5R)-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid, has several potential applications in the field of organic synthesis and pharmaceutical research.Firstly, the compound belongs to the oxazolidine family, which is known for its versatile reactivity. Oxazolidines are often utilized as chiral auxiliaries, aiding in the asymmetric synthesis of organic molecules. As a chiral auxiliary, (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid can be used to control stereochemistry in various reactions. It can act as a protecting group or a chiral template, facilitating the formation of desired enantiomers in a reaction sequence.Furthermore, the compound's tert-butoxycarbonyl (Boc) protecting group offers stability and selectivity in organic reactions. Boc groups are commonly used to protect amino groups, preventing undesired reactions and allowing for selective functionalizations. During the synthesis of peptides or other organic compounds containing amino groups, (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid can serve as a protecting group to shield the amine functionality until further manipulation is required.In addition to its use as a chiral auxiliary and protecting group, (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid may possess biological activity or be a precursor to biologically active compounds. Further research and investigation are needed to fully explore its potential in the field of medicinal chemistry.It is important to note that the specific application and use of (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid may vary depending on the desired chemical reaction, the target molecule, and the objectives of the synthetic or pharmaceutical endeavor.In summary, (4S,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid is a versatile compound with potential uses in asymmetric synthesis, protecting group chemistry, and pharmaceutical research. Its chiral nature, stability as a protecting group, and potential biological activity make it an interesting building block for the development of novel compounds and the synthesis of complex organic molecules.