cis-(1R,2S)-2-Aminocyclopentanol hydrochloride

98%

Reagent Code: #229813
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Alias Cis-(1R,2S)-2-aminocyclopentyl alcohol hydrochloride
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CAS Number 137254-03-6

science Other reagents with same CAS 137254-03-6

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Weight 137.61 g/mol
Formula C₅H₁₁NO·HCl
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MDL Number MFCD07370091
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antitumor agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the preparation of cyclopentane-based nucleoside analogs, which mimic natural nucleosides and interfere with viral replication. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties of drug candidates due to its favorable polarity and hydrogen bonding capacity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,880.00
inventory 5g
10-20 days ฿6,880.00
inventory 25g
10-20 days ฿22,860.00

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cis-(1R,2S)-2-Aminocyclopentanol hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antitumor agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the preparation of cyclopentane-based nucleoside analogs, which mimic natural nucleosides and interfere with viral replication. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties of drug candidates due to its fav

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral and antitumor agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Commonly employed in the preparation of cyclopentane-based nucleoside analogs, which mimic natural nucleosides and interfere with viral replication. Also utilized in medicinal chemistry for optimizing pharmacokinetic properties of drug candidates due to its favorable polarity and hydrogen bonding capacity.

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