(S)-tert-Butyl 2-(3-bromophenyl)pyrrolidine-1-carboxylate
97%
- Product Code: 71118
CAS:
2061996-90-3
| Molecular Weight: | 326.23 g./mol | Molecular Formula: | C₁₁H₂₂O₂ |
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| EC Number: | MDL Number: | MFCD30609559 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure, featuring a pyrrolidine ring and a bromophenyl group, makes it a valuable intermediate in the construction of complex molecules. It is often employed in asymmetric synthesis to create chiral compounds, which are essential in the production of drugs with specific stereochemical requirements. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the preparation of compounds for biological studies, such as enzyme inhibitors or receptor modulators. Its bromine atom also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $311.07 |
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| 0.250 | 10-20 days | $622.41 |
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(S)-tert-Butyl 2-(3-bromophenyl)pyrrolidine-1-carboxylate
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive compounds. Its structure, featuring a pyrrolidine ring and a bromophenyl group, makes it a valuable intermediate in the construction of complex molecules. It is often employed in asymmetric synthesis to create chiral compounds, which are essential in the production of drugs with specific stereochemical requirements. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the preparation of compounds for biological studies, such as enzyme inhibitors or receptor modulators. Its bromine atom also allows for further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry and material science.
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