(S)-3-Ethoxypyrrolidine

97%

Reagent Code: #38424
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CAS Number 143943-75-3

science Other reagents with same CAS 143943-75-3

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Weight 115.1760 g/mol
Formula C₆H₁₃NO
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MDL Number MFCD00800372
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(S)-3-Ethoxypyrrolidine is primarily utilized as a chiral building block in the synthesis of various pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure compounds, particularly in the production of drugs targeting the central nervous system. The compound is often employed in the creation of active pharmaceutical ingredients (APIs) for treatments related to neurological disorders, such as Parkinson's disease and depression. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, where its ethoxy group can be further modified to introduce specific functionalities. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new therapeutic agents with enhanced efficacy and selectivity.

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inventory 100mg
10-20 days ฿2,259.00

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(S)-3-Ethoxypyrrolidine
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(S)-3-Ethoxypyrrolidine is primarily utilized as a chiral building block in the synthesis of various pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure compounds, particularly in the production of drugs targeting the central nervous system. The compound is often employed in the creation of active pharmaceutical ingredients (APIs) for treatments related to neurological disorders, such as Parkinson's disease and depression. Additionally, it serves as a key in

(S)-3-Ethoxypyrrolidine is primarily utilized as a chiral building block in the synthesis of various pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure compounds, particularly in the production of drugs targeting the central nervous system. The compound is often employed in the creation of active pharmaceutical ingredients (APIs) for treatments related to neurological disorders, such as Parkinson's disease and depression. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, where its ethoxy group can be further modified to introduce specific functionalities. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new therapeutic agents with enhanced efficacy and selectivity.

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