(S)-2-Amino-3-(benzyloxy)propan-1-ol hydrochloride

95%

Reagent Code: #236253
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CAS Number 61366-43-6

science Other reagents with same CAS 61366-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.69 g/mol
Formula C₁₀H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD07368914
inventory_2 Storage & Handling
Storage Room temperature, inert atmosphere

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its hydroxyl and amino functional groups allow for versatile chemical modifications, making it valuable in asymmetric synthesis. The compound is also employed in the preparation of enzyme inhibitors and bioactive molecules where stereochemistry plays a critical role in biological activity. Commonly utilized in medicinal chemistry for structure-activity relationship studies due to its rigid backbone and defined stereoconfiguration.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,490.00
inventory 250mg
10-20 days ฿5,240.00
inventory 1g
10-20 days ฿12,960.00
(S)-2-Amino-3-(benzyloxy)propan-1-ol hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its hydroxyl and amino functional groups allow for versatile chemical modifications, making it valuable in asymmetric synthesis. The compound is also employed in the preparation of enzyme inhibitors and bioactive molecules where stereochemistry plays a critical role in biological activity. Commonly utilized in medicinal chemistry for structure-activity relation

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its hydroxyl and amino functional groups allow for versatile chemical modifications, making it valuable in asymmetric synthesis. The compound is also employed in the preparation of enzyme inhibitors and bioactive molecules where stereochemistry plays a critical role in biological activity. Commonly utilized in medicinal chemistry for structure-activity relationship studies due to its rigid backbone and defined stereoconfiguration.

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