(S)-4-(Pyrrolidin-2-yl)benzoic acid hydrochloride

95%(HPLC)

Reagent Code: #233226
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CAS Number 1381927-91-8

science Other reagents with same CAS 1381927-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.69 g/mol
Formula C₁₁H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD12758939
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of neuroactive agents due to the presence of a pyrrolidine ring linked to an aromatic system, which is common in central nervous system-targeting drugs. Frequently employed in the preparation of serotonin and dopamine receptor ligands. Also utilized in asymmetric synthesis where stereochemistry plays a critical role in drug efficacy. Its hydrochloride salt form improves solubility and stability, making it suitable for solution-phase reactions in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,550.00
inventory 250mg
10-20 days ฿40,030.00

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(S)-4-(Pyrrolidin-2-yl)benzoic acid hydrochloride
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Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of neuroactive agents due to the presence of a pyrrolidine ring linked to an aromatic system, which is common in central nervous system-targeting drugs. Frequently employed in the preparation of serotonin and dopamine receptor ligands. Also utilized in asymmetric synthesis where stereochemistry plays a critical role in drug efficacy. Its hydrochloride salt form

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of neuroactive agents due to the presence of a pyrrolidine ring linked to an aromatic system, which is common in central nervous system-targeting drugs. Frequently employed in the preparation of serotonin and dopamine receptor ligands. Also utilized in asymmetric synthesis where stereochemistry plays a critical role in drug efficacy. Its hydrochloride salt form improves solubility and stability, making it suitable for solution-phase reactions in medicinal chemistry.

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