(R)-Benzyl (2-amino-1-phenylethyl)carbamate

95%

Reagent Code: #37281
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CAS Number 130406-35-8

science Other reagents with same CAS 130406-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.3263 g/mol
Formula C₁₆H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD09260583
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. Its structure is valuable in the development of beta-blockers and other cardiovascular medications, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in asymmetric synthesis to create complex molecules with high optical purity, which is essential for drug development and research. Its carbamate group also makes it a useful protecting group for amines in multi-step organic synthesis.

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inventory 100mg
10-20 days ฿6,255.00

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(R)-Benzyl (2-amino-1-phenylethyl)carbamate
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This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. Its structure is valuable in the development of beta-blockers and other cardiovascular medications, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in asymmetric synthesis to create complex molecules with high optical pu

This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceutical applications. It serves as a key building block in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. Its structure is valuable in the development of beta-blockers and other cardiovascular medications, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in asymmetric synthesis to create complex molecules with high optical purity, which is essential for drug development and research. Its carbamate group also makes it a useful protecting group for amines in multi-step organic synthesis.

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