N-Boc-D-phenylalaninol

97%

Reagent Code: #216606
label
Alias N-(tert-butoxycarbonyl)-D-phenylalanol, (R)-2-(Boc-amino)-3-phenyl-1-propanol, R)-2-(tert-butoxycarbonyl)-3-phenyl-1-propanol
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CAS Number 106454-69-7

science Other reagents with same CAS 106454-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.32 g/mol
Formula C₁₄H₂₁NO₃
badge Registry Numbers
MDL Number MFCD00216472
thermostat Physical Properties
Melting Point 95-98 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its Boc-protected amine and alcohol functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis and resolution processes due to the stability and stereochemical integrity of the D-configuration. Also utilized in the preparation of peptidomimetics and as a building block in combinatorial chemistry for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿1,330.00
100g
10-20 days ฿5,190.00
500g
10-20 days ฿19,460.00
N-Boc-D-phenylalaninol
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Used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its Boc-protected amine and alcohol functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis and resolution processes due to the stability and stereochemical integrity of the D-configuration. Also utilized in the preparation of peptidomimetics and as a building block in combinatorial chemistry

Used in the synthesis of chiral intermediates for pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its Boc-protected amine and alcohol functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis and resolution processes due to the stability and stereochemical integrity of the D-configuration. Also utilized in the preparation of peptidomimetics and as a building block in combinatorial chemistry for drug discovery.

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