(R)-Methyl 2-(pyrrolidin-3-yl)acetate hydrochloride

98%

Reagent Code: #37508
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CAS Number 1024038-31-0

science Other reagents with same CAS 1024038-31-0

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scatter_plot Molecular Information
Weight 179.6446 g/mol
Formula C₇H₁₄ClNO₂
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MDL Number MFCD22377963
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description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral molecules. Its structure, featuring a pyrrolidine ring and an ester group, makes it a valuable intermediate in the production of drugs targeting the central nervous system. It is often employed in the creation of compounds with potential therapeutic effects on neurological disorders, such as Parkinson's disease or cognitive impairments. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects. The hydrochloride salt form improves its stability and solubility, facilitating its use in various chemical reactions and formulations.

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inventory 100mg
10-20 days ฿2,835.00

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(R)-Methyl 2-(pyrrolidin-3-yl)acetate hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral molecules. Its structure, featuring a pyrrolidine ring and an ester group, makes it a valuable intermediate in the production of drugs targeting the central nervous system. It is often employed in the creation of compounds with potential therapeutic effects on neurological disorders, such as Parkinson's disease or cognitive impairments. Additionally, its chiral nature allows for the developm

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral molecules. Its structure, featuring a pyrrolidine ring and an ester group, makes it a valuable intermediate in the production of drugs targeting the central nervous system. It is often employed in the creation of compounds with potential therapeutic effects on neurological disorders, such as Parkinson's disease or cognitive impairments. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects. The hydrochloride salt form improves its stability and solubility, facilitating its use in various chemical reactions and formulations.

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