(R)-2-Amino-2-(tetrahydro-2H-pyran-4-yl)acetic acid

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Reagent Code: #230078
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CAS Number 475649-32-2

science Other reagents with same CAS 475649-32-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.18 g/mol
Formula C₇H₁₃NO₃
badge Registry Numbers
MDL Number MFCD01631205
thermostat Physical Properties
Boiling Point 316.7±17.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C virus (HCV) protease inhibitors. Its structural features enable high selectivity and binding affinity in pharmaceutical agents targeting viral replication. The compound's stereochemistry plays a critical role in enhancing drug efficacy and metabolic stability. It is also employed in the development of other biologically active molecules where a constrained cyclic ether and amino acid functionality are required for activity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿890.00
inventory 100mg
10-20 days ฿2,130.00
inventory 250mg
10-20 days ฿3,070.00
inventory 1g
10-20 days ฿10,670.00
inventory 5g
10-20 days ฿53,310.00

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(R)-2-Amino-2-(tetrahydro-2H-pyran-4-yl)acetic acid
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Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C virus (HCV) protease inhibitors. Its structural features enable high selectivity and binding affinity in pharmaceutical agents targeting viral replication. The compound's stereochemistry plays a critical role in enhancing drug efficacy and metabolic stability. It is also employed in the development of other biologically active molecules where a constrained cyclic ether and amino acid funct

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C virus (HCV) protease inhibitors. Its structural features enable high selectivity and binding affinity in pharmaceutical agents targeting viral replication. The compound's stereochemistry plays a critical role in enhancing drug efficacy and metabolic stability. It is also employed in the development of other biologically active molecules where a constrained cyclic ether and amino acid functionality are required for activity.

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