trans-(1S,2S)-2-Aminocyclopentanol hydrochloride

98%

Reagent Code: #234210
label
Alias Trans-(1S,2S)-2-aminocyclopentyl hydrochloride
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CAS Number 68327-04-8

science Other reagents with same CAS 68327-04-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.61 g/mol
Formula C₅H₁₁NO·HCl
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MDL Number MFCD07370092
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid cyclopentane backbone and functional groups (amino and hydroxyl) allow for selective derivatization, making it valuable in the development of enzyme inhibitors and receptor agonists/antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its defined spatial orientation of functional groups. Also utilized in asymmetric synthesis as a precursor to chiral ligands or organocatalysts.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿774.00
inventory 25g
10-20 days ฿3,858.00

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trans-(1S,2S)-2-Aminocyclopentanol hydrochloride
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid cyclopentane backbone and functional groups (amino and hydroxyl) allow for selective derivatization, making it valuable in the development of enzyme inhibitors and receptor agonists/antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its defined spatial orientation of functional

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its rigid cyclopentane backbone and functional groups (amino and hydroxyl) allow for selective derivatization, making it valuable in the development of enzyme inhibitors and receptor agonists/antagonists. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its defined spatial orientation of functional groups. Also utilized in asymmetric synthesis as a precursor to chiral ligands or organocatalysts.

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