(1S,3S)-3-Aminocyclopentanol hydrochloride

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Reagent Code: #36266
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CAS Number 1523530-42-8

science Other reagents with same CAS 1523530-42-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.61 g/mol
Formula C₅H₁₂ClNO
badge Registry Numbers
MDL Number MFCD23704943
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

(1S,3S)-3-Aminocyclopentanol hydrochloride is primarily used in pharmaceutical research and development as a chiral building block or intermediate in the synthesis of more complex molecules. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial in drug design to ensure specificity and reduce side effects. It is often employed in the preparation of bioactive molecules, including potential therapeutics for neurological disorders, due to its structural similarity to certain neurotransmitters. Additionally, it may be utilized in the development of ligands for asymmetric catalysis, aiding in the production of chiral drugs or fine chemicals. Its hydrochloride form enhances solubility, making it suitable for various reaction conditions in organic synthesis.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿26,604.00
inventory 1g
10-20 days ฿9,072.00
inventory 250mg
10-20 days ฿3,924.00

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(1S,3S)-3-Aminocyclopentanol hydrochloride
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(1S,3S)-3-Aminocyclopentanol hydrochloride is primarily used in pharmaceutical research and development as a chiral building block or intermediate in the synthesis of more complex molecules. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial in drug design to ensure specificity and reduce side effects. It is often employed in the preparation of bioactive molecules, including potential therapeutics for neurological disorders, due to its structural similar

(1S,3S)-3-Aminocyclopentanol hydrochloride is primarily used in pharmaceutical research and development as a chiral building block or intermediate in the synthesis of more complex molecules. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial in drug design to ensure specificity and reduce side effects. It is often employed in the preparation of bioactive molecules, including potential therapeutics for neurological disorders, due to its structural similarity to certain neurotransmitters. Additionally, it may be utilized in the development of ligands for asymmetric catalysis, aiding in the production of chiral drugs or fine chemicals. Its hydrochloride form enhances solubility, making it suitable for various reaction conditions in organic synthesis.

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