(R)-2-(2-Fluorophenyl)pyrrolidine hydrochloride

95%

Reagent Code: #87149
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CAS Number 1381929-34-5

science Other reagents with same CAS 1381929-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.67 g/mol
Formula C₁₀H₁₃ClFN
badge Registry Numbers
MDL Number MFCD08751399
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a pyrrolidine ring, makes it valuable for developing pharmaceuticals targeting the central nervous system. It is often employed in the creation of compounds with potential therapeutic effects on neurological disorders, such as depression, anxiety, and cognitive impairments. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug design, enhancing the specificity and efficacy of potential treatments. Researchers also use it in the study of receptor binding and enzyme inhibition, contributing to the development of novel drugs with improved safety profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,212.00

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(R)-2-(2-Fluorophenyl)pyrrolidine hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a pyrrolidine ring, makes it valuable for developing pharmaceuticals targeting the central nervous system. It is often employed in the creation of compounds with potential therapeutic effects on neurological disorders, such as depression, anxiety, and cognitive impairments. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug design, enhancing the specificity and efficacy of potential treatments. Researchers also use it in the study of receptor binding and enzyme inhibition, contributing to the development of novel drugs with improved safety profiles.
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