(1S,2R,4R)-4-(Boc-amino)-2-(hydroxymethyl)cyclopentanol

95%

Reagent Code: #82791
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CAS Number 153045-91-1

science Other reagents with same CAS 153045-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₁H₂₁NO₄
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, enabling precise modifications during the synthesis process. Additionally, its cyclopentanol structure contributes to the stability and bioavailability of the final drug compounds. It is also employed in research settings for studying enzyme interactions and metabolic pathways, aiding in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,800.00
inventory 250mg
10-20 days ฿38,700.00

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(1S,2R,4R)-4-(Boc-amino)-2-(hydroxymethyl)cyclopentanol
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, enabling precise modifications during the synthesis process. Additionally, its cyclopentanol structure contributes to the stability and bioavailabil

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, enabling precise modifications during the synthesis process. Additionally, its cyclopentanol structure contributes to the stability and bioavailability of the final drug compounds. It is also employed in research settings for studying enzyme interactions and metabolic pathways, aiding in the discovery of new therapeutic agents.

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