1-(4-Bromo-2-tert-butylphenyl)pyrrolidine
97%
- Product Code: 68153
CAS:
850012-53-2
| Molecular Weight: | 282.22 g./mol | Molecular Formula: | C₁₄H₂₀BrN |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 340.1±35.0 °C(Predicted) | |
| Density: | 1.244±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex chemical structures. Its unique structure, featuring a pyrrolidine ring and a bromo-substituted phenyl group, makes it valuable for constructing molecules with specific pharmacological properties. It is often employed in the development of active pharmaceutical ingredients (APIs) for drugs targeting neurological and psychiatric disorders. Additionally, its tert-butyl group enhances steric hindrance, which can be advantageous in designing compounds with improved selectivity and stability. Researchers also use it in the study of ligand-receptor interactions, particularly in the development of receptor modulators. Its versatility in chemical reactions, such as cross-coupling and cyclization, further broadens its application in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿20,790.00 |
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| 1.000 | 10-20 days | ฿31,248.00 |
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1-(4-Bromo-2-tert-butylphenyl)pyrrolidine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex chemical structures. Its unique structure, featuring a pyrrolidine ring and a bromo-substituted phenyl group, makes it valuable for constructing molecules with specific pharmacological properties. It is often employed in the development of active pharmaceutical ingredients (APIs) for drugs targeting neurological and psychiatric disorders. Additionally, its tert-butyl group enhances steric hindrance, which can be advantageous in designing compounds with improved selectivity and stability. Researchers also use it in the study of ligand-receptor interactions, particularly in the development of receptor modulators. Its versatility in chemical reactions, such as cross-coupling and cyclization, further broadens its application in medicinal chemistry and drug discovery.
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