AE10887
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $96.00 | $67.00 | - + | |
500mg | 95% | in stock | $160.00 | $112.00 | - + | |
1g | 95% | in stock | $240.00 | $168.00 | - + | |
5g | 95% | in stock | $758.00 | $531.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE10887 |
Chemical Name: | (S)-tert-Butyl 3-(chloromethyl)pyrrolidine-1-carboxylate |
CAS Number: | 1187932-75-7 |
Molecular Formula: | C10H18ClNO2 |
Molecular Weight: | 219.7084 |
MDL Number: | MFCD08059336 |
SMILES: | ClC[C@H]1CCN(C1)C(=O)OC(C)(C)C |
Complexity: | 213 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 3 |
XLogP3: | 2.1 |
1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate is a versatile compound commonly used in chemical synthesis for a variety of applications. Its primary role lies in the realm of organic chemistry, where it serves as a valuable building block in the creation of complex molecules and pharmaceuticals. This compound's unique structure enables it to participate in a range of important reactions, including nucleophilic substitutions, rearrangements, and reductions. Chemists often utilize 1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate to introduce specific functional groups or motifs into target molecules, thereby facilitating the synthesis of intricate molecular structures with precision and efficiency. In addition to its synthetic utility, this compound's chirality (specifically the (3S) stereochemistry) allows for the creation of enantiomerically pure products, which is crucial in the pharmaceutical industry and other fields requiring high levels of stereochemical control. Overall, 1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate plays a crucial role in advancing chemical synthesis by enabling the construction of diverse and complex molecular architectures with strategic control over stereochemistry and functionality.