(R)-tert-Butyl (1-(4-(benzyloxy)phenyl)-3-hydroxypropan-2-yl)carbamate

95%

Reagent Code: #228657
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CAS Number 198470-63-2

science Other reagents with same CAS 198470-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.44 g/mol
Formula C₂₁H₂₇NO₄
badge Registry Numbers
MDL Number MFCD00235957
thermostat Physical Properties
Boiling Point 536.1±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.130±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in multi-step organic syntheses where stereochemistry is critical for biological activity. The benzyl ether group serves as a protecting group that can be removed under mild conditions, making it suitable for use in sensitive reaction sequences.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,810.00
inventory 1g
10-20 days ฿12,800.00
(R)-tert-Butyl (1-(4-(benzyloxy)phenyl)-3-hydroxypropan-2-yl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in multi-step organic syntheses where stereochemistry is critical for biological activity. The benzyl ether group serves as a protecting group that can be removed under m
Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carbamate functional groups allow for selective chemical modifications, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in multi-step organic syntheses where stereochemistry is critical for biological activity. The benzyl ether group serves as a protecting group that can be removed under mild conditions, making it suitable for use in sensitive reaction sequences.
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