4,4-Dimethylpyrrolidine-3-carboxylic acid hydrochloride

≥95%

Reagent Code: #45836
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CAS Number 1351343-41-3

science Other reagents with same CAS 1351343-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.65 g/mol
Formula C₇H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD19686958
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the development of drugs targeting neurological disorders due to its structural similarity to certain neurotransmitters. Additionally, it plays a role in the preparation of chiral catalysts, which are essential in asymmetric synthesis for producing enantiomerically pure compounds. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous reaction environments.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,586.00
inventory 250mg
10-20 days ฿7,029.00
inventory 100mg
10-20 days ฿4,689.00

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4,4-Dimethylpyrrolidine-3-carboxylic acid hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the development of drugs targeting neurological disorders due to its structural similarity to certain neurotransmitters. Additionally, it plays a role in the preparation of chiral catalysts, which are essential in asymmetric synthesis for producing enantiomerically pure compounds. Its hydrochloride form enhances solubility, making it more su

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the development of drugs targeting neurological disorders due to its structural similarity to certain neurotransmitters. Additionally, it plays a role in the preparation of chiral catalysts, which are essential in asymmetric synthesis for producing enantiomerically pure compounds. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous reaction environments.

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