Ethyl 2-(pyrrolidin-3-yl)acetate hydrochloride

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Reagent Code: #182669
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CAS Number 726139-60-2

science Other reagents with same CAS 726139-60-2

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Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a pharmaceutical intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with neurological activity, including those targeting cognitive enhancement and neurodegenerative disorders. Commonly utilized in research settings for designing nootropic drugs and serotonin receptor modulators. Also serves as a building block in the preparation of pyrrolidine-based bioactive molecules due to its functionalized backbone that facilitates chemical modifications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿890.00
inventory 250mg
10-20 days ฿1,890.00
inventory 1g
10-20 days ฿5,600.00

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Ethyl 2-(pyrrolidin-3-yl)acetate hydrochloride
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Used primarily as a pharmaceutical intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with neurological activity, including those targeting cognitive enhancement and neurodegenerative disorders. Commonly utilized in research settings for designing nootropic drugs and serotonin receptor modulators. Also serves as a building block in the preparation of pyrrolidine

Used primarily as a pharmaceutical intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with neurological activity, including those targeting cognitive enhancement and neurodegenerative disorders. Commonly utilized in research settings for designing nootropic drugs and serotonin receptor modulators. Also serves as a building block in the preparation of pyrrolidine-based bioactive molecules due to its functionalized backbone that facilitates chemical modifications.

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