(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride

97%

Reagent Code: #71078
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CAS Number 623583-10-8

science Other reagents with same CAS 623583-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.59 g/mol
Formula C₅H₁₀ClF₂NO
badge Registry Numbers
MDL Number MFCD22570251
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride is primarily utilized in pharmaceutical research and development as a chiral building block. Its structure, featuring a difluorinated pyrrolidine ring, makes it valuable for synthesizing bioactive molecules, particularly in the design of drugs targeting the central nervous system (CNS). The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is critical for optimizing drug efficacy and reducing side effects. It is often employed in the synthesis of potential therapeutic agents for neurological disorders, such as Parkinson’s disease or schizophrenia, due to its ability to interact with specific receptors or enzymes in the brain. Additionally, its fluorine atoms enhance metabolic stability and bioavailability, making it a preferred intermediate in medicinal chemistry.

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inventory 100mg
10-20 days ฿3,582.00

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(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride
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(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride is primarily utilized in pharmaceutical research and development as a chiral building block. Its structure, featuring a difluorinated pyrrolidine ring, makes it valuable for synthesizing bioactive molecules, particularly in the design of drugs targeting the central nervous system (CNS). The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is critical for optimizing drug efficacy and reducing side effects. I

(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride is primarily utilized in pharmaceutical research and development as a chiral building block. Its structure, featuring a difluorinated pyrrolidine ring, makes it valuable for synthesizing bioactive molecules, particularly in the design of drugs targeting the central nervous system (CNS). The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is critical for optimizing drug efficacy and reducing side effects. It is often employed in the synthesis of potential therapeutic agents for neurological disorders, such as Parkinson’s disease or schizophrenia, due to its ability to interact with specific receptors or enzymes in the brain. Additionally, its fluorine atoms enhance metabolic stability and bioavailability, making it a preferred intermediate in medicinal chemistry.

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