AA54110
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $105.00 | $74.00 | - + | |
250mg | 98% | in stock | $177.00 | $124.00 | - + | |
1g | 98% | in stock | $437.00 | $306.00 | - + | |
5g | 98% | in stock | $1,287.00 | $901.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA54110 |
Chemical Name: | (2S)-2-(3-Bromophenyl)pyrrolidine |
CAS Number: | 1217694-15-9 |
Molecular Formula: | C10H12BrN |
Molecular Weight: | 226.11298000000008 |
MDL Number: | MFCD06762566 |
SMILES: | Brc1cccc(c1)[C@@H]1CCCN1 |
Complexity: | 149 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 1 |
XLogP3: | 2.5 |
(S)-2-(3-Bromophenyl)pyrrolidine is a versatile compound that finds extensive application in chemical synthesis. As a chiral building block, this compound plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and chirality make it a valuable intermediate in asymmetric synthesis, enabling the creation of enantiomerically pure compounds.In organic chemistry, (S)-2-(3-Bromophenyl)pyrrolidine is often used as a key starting material for the synthesis of complex molecules with defined stereochemistry. Its presence allows for the introduction of the 3-bromophenyl group into organic frameworks, facilitating the formation of new bonds and the construction of diverse molecular architectures. This compound's incorporation can impart specific biological activities or physical properties to the final products, making it an essential tool for the design and development of novel chemical entities.Furthermore, (S)-2-(3-Bromophenyl)pyrrolidine serves as a valuable reagent in cross-coupling reactions, ring-closure reactions, and other transformations that require the presence of a pyrrolidine moiety. Its controlled chirality enables chemists to access enantioenriched compounds with high selectivity and efficiency, showcasing its significance in the field of asymmetric synthesis. By harnessing the synthetic potential of (S)-2-(3-Bromophenyl)pyrrolidine, researchers can advance the frontiers of chemical science and create innovative solutions for various applications.