cis-dimethyl pyrrolidine-3,4-dicarboxylate hydrochloride

98%

Reagent Code: #55134
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CAS Number 102389-89-9

science Other reagents with same CAS 102389-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.65 g/mol
Formula C₈H₁₄ClNO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Primarily utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological disorders, as it can be modified to enhance blood-brain barrier penetration. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry is crucial for producing enantiomerically pure substances. In medicinal chemistry, it is often used to explore structure-activity relationships (SAR) for optimizing drug efficacy and minimizing side effects. Its hydrochloride form ensures better solubility and stability, making it suitable for experimental and industrial applications.

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Test Parameter Specification
Appearance White Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,080.00
inventory 100mg
10-20 days ฿3,990.00

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cis-dimethyl pyrrolidine-3,4-dicarboxylate hydrochloride
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Primarily utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological disorders, as it can be modified to enhance blood-brain barrier penetration. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry is crucial for producing enantiomerically pure substances. In medicinal chemistry, it is o
Primarily utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological disorders, as it can be modified to enhance blood-brain barrier penetration. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry is crucial for producing enantiomerically pure substances. In medicinal chemistry, it is often used to explore structure-activity relationships (SAR) for optimizing drug efficacy and minimizing side effects. Its hydrochloride form ensures better solubility and stability, making it suitable for experimental and industrial applications.
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