(R)-tert-Butyl (1-(2-nitrophenyl)ethyl)carbamate

95%

Reagent Code: #37270
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CAS Number 2411591-10-9

science Other reagents with same CAS 2411591-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.2930 g/mol
Formula C₁₃H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD32062605
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 neurological and cardiovascular disorders. Its structure is advantageous in asymmetric synthesis, enabling the creation of complex molecules with high stereochemical control. Additionally, it is employed in research and development for designing novel therapeutic agents, leveraging its nitro and carbamate functional groups for further chemical modifications. Its stability and reactivity make it a valuable reagent in organic synthesis and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,963.00

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(R)-tert-Butyl (1-(2-nitrophenyl)ethyl)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 neurological and cardiovascular disorders. Its structure is advantageous in asymmetric synthesis, enabling the creation of complex molecules with high stereochemical control. Additionally, it is employed in research and development for designing novel therapeutic agents, leveraging its

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 neurological and cardiovascular disorders. Its structure is advantageous in asymmetric synthesis, enabling the creation of complex molecules with high stereochemical control. Additionally, it is employed in research and development for designing novel therapeutic agents, leveraging its nitro and carbamate functional groups for further chemical modifications. Its stability and reactivity make it a valuable reagent in organic synthesis and medicinal chemistry.

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