1-(4-Bromo-2-tert-butylphenyl)pyrrolidine

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Reagent Code: #68153
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CAS Number 850012-53-2

science Other reagents with same CAS 850012-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.22 g/mol
Formula C₁₄H₂₀BrN
thermostat Physical Properties
Boiling Point 340.1±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.244±0.06 g/cm3(Predicted)
Storage room temperature, dry

description 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.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿31,248.00
inventory 500mg
10-20 days ฿20,790.00

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1-(4-Bromo-2-tert-butylphenyl)pyrrolidine
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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-bu

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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