(S)-3-Amino-3-cyclopentylpropanoic acid hydrochloride

≥95%

Reagent Code: #38450
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CAS Number 1956435-02-1

science Other reagents with same CAS 1956435-02-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD27920773
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure, featuring a cyclopentyl group and an amino acid moiety, makes it valuable in the development of drugs targeting neurological disorders, such as epilepsy and neurodegenerative diseases. Additionally, it serves as a building block in the creation of peptide-based drugs, where its chiral center ensures the production of enantiomerically pure compounds. The hydrochloride form enhances its solubility, facilitating its use in various chemical reactions and formulations. Its application extends to research settings, where it is employed in the study of enzyme inhibition and receptor binding mechanisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿39,375.00

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(S)-3-Amino-3-cyclopentylpropanoic acid hydrochloride
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure, featuring a cyclopentyl group and an amino acid moiety, makes it valuable in the development of drugs targeting neurological disorders, such as epilepsy and neurodegenerative diseases. Additionally, it serves as a building block in the creation of peptide-based drugs, where its chiral center ensures the production of enantiomerically pure compounds. The h

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure, featuring a cyclopentyl group and an amino acid moiety, makes it valuable in the development of drugs targeting neurological disorders, such as epilepsy and neurodegenerative diseases. Additionally, it serves as a building block in the creation of peptide-based drugs, where its chiral center ensures the production of enantiomerically pure compounds. The hydrochloride form enhances its solubility, facilitating its use in various chemical reactions and formulations. Its application extends to research settings, where it is employed in the study of enzyme inhibition and receptor binding mechanisms.

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