2-(2-Bromophenyl)pyrrolidine hydrochloride

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Reagent Code: #152122
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CAS Number 1197232-93-1

science Other reagents with same CAS 1197232-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.57 g/mol
Formula C₁₀H₁₃BrClN
badge Registry Numbers
MDL Number MFCD08456883
inventory_2 Storage & Handling
Storage Room temperature, sealed, light-proof

description Product Description

Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of chiral catalysts and ligands in asymmetric synthesis. Commonly employed in the preparation of neuroactive agents due to the pyrrolidine core, which is prevalent in central nervous system drugs. Also utilized in research settings for the construction of complex heterocyclic systems through cross-coupling reactions, particularly in palladium-catalyzed transformations involving the bromoaryl group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿460.00
inventory 250mg
10-20 days ฿1,060.00
inventory 1g
10-20 days ฿4,030.00

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2-(2-Bromophenyl)pyrrolidine hydrochloride
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Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of chiral catalysts and ligands in asymmetric synthesis. Commonly employed in the preparation of neuroactive agents due to the pyrrolidine core, which is prevalent in central nervous system drugs. Also utilized in research settings for the construction of complex heterocyclic systems through cross-coupling reactions, particularly in palladium-catalyzed trans

Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of chiral catalysts and ligands in asymmetric synthesis. Commonly employed in the preparation of neuroactive agents due to the pyrrolidine core, which is prevalent in central nervous system drugs. Also utilized in research settings for the construction of complex heterocyclic systems through cross-coupling reactions, particularly in palladium-catalyzed transformations involving the bromoaryl group.

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