(R)-tert-Butyl (1-(5-bromopyridin-2-yl)-2-hydroxyethyl)carbamate

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Reagent Code: #37272
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CAS Number 2126088-15-9

science Other reagents with same CAS 2126088-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.18 g/mol
Formula C₁₂H₁₇BrN₂O₃
badge Registry Numbers
MDL Number MFCD31539627
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a bromopyridine moiety and a protected amino alcohol group, makes it a valuable building block in the creation of biologically active molecules. It is often employed in the preparation of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas. The chiral center allows for the development of enantiomerically pure drugs, which is crucial for optimizing efficacy and reducing side effects. Additionally, its bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the construction of more complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,062.00
inventory 100mg
10-20 days ฿14,031.00

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(R)-tert-Butyl (1-(5-bromopyridin-2-yl)-2-hydroxyethyl)carbamate
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a bromopyridine moiety and a protected amino alcohol group, makes it a valuable building block in the creation of biologically active molecules. It is often employed in the preparation of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas. The chiral center allows for the development

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a bromopyridine moiety and a protected amino alcohol group, makes it a valuable building block in the creation of biologically active molecules. It is often employed in the preparation of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas. The chiral center allows for the development of enantiomerically pure drugs, which is crucial for optimizing efficacy and reducing side effects. Additionally, its bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the construction of more complex molecular architectures.

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