AA13802
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 96% | in stock | $72.00 | $50.00 | - + | |
1g | 96% | in stock | $155.00 | $108.00 | - + | |
5g | 96% | in stock | $440.00 | $308.00 | - + | |
25g | 96% | in stock | $1,955.00 | $1,369.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA13802 |
Chemical Name: | tert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylate |
CAS Number: | 114214-70-9 |
Molecular Formula: | C17H25NO5S |
Molecular Weight: | 355.4491 |
MDL Number: | MFCD08704608 |
SMILES: | Cc1ccc(cc1)S(=O)(=O)OCC1CCN(C1)C(=O)OC(C)(C)C |
The tert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. Its unique structure and reactivity make it an invaluable building block for the synthesis of various complex molecules and pharmaceutical intermediates.One of the primary applications of tert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylate is as a protecting group in organic synthesis. Due to the presence of the tosyl group, this compound can selectively mask reactive functional groups in complex molecules, allowing chemists to carry out specific reactions without affecting other parts of the molecule. This property makes it an essential tool in the synthesis of intricate organic compounds, where multiple reactive sites are present.Additionally, tert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylate can act as a nucleophilic catalyst in certain reactions, facilitating the formation of new carbon-carbon bonds or other key transformations. Its high reactivity and stability under various reaction conditions make it a highly sought-after reagent in the realm of chemical synthesis.Overall, the tert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylate plays a critical role in enabling chemists to access new chemical entities and complex molecules through strategic manipulation of functional groups and reactivity profiles. Its versatility and utility make it a cornerstone in the toolkit of synthetic chemists striving to create novel compounds for a wide range of applications.