(1R,3S)-3-Aminocyclopentanol

98%

Reagent Code: #229296
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CAS Number 1110772-05-8

science Other reagents with same CAS 1110772-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD11052498
thermostat Physical Properties
Boiling Point 179 °C
inventory_2 Storage & Handling
Density 1.084 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiviral and central nervous system agents. Its rigid cyclopentane backbone and functional groups in defined stereochemistry make it valuable for designing enzyme inhibitors and receptor-targeted drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies where stereochemistry influences biological activity. Also utilized in the preparation of conformationally constrained analogs of bioactive molecules to enhance metabolic stability and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,420.00
250mg
10-20 days ฿10,910.00
1g
10-20 days ฿29,420.00
(1R,3S)-3-Aminocyclopentanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiviral and central nervous system agents. Its rigid cyclopentane backbone and functional groups in defined stereochemistry make it valuable for designing enzyme inhibitors and receptor-targeted drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies where stereochemistry influences biological activity. Also utilized in the preparation of conformationally constrain

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiviral and central nervous system agents. Its rigid cyclopentane backbone and functional groups in defined stereochemistry make it valuable for designing enzyme inhibitors and receptor-targeted drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies where stereochemistry influences biological activity. Also utilized in the preparation of conformationally constrained analogs of bioactive molecules to enhance metabolic stability and selectivity.

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