tert-Butyl (2-bromopyrimidin-5-yl)carbamate

98%

Reagent Code: #146692
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CAS Number 1314390-34-5

science Other reagents with same CAS 1314390-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.11 g/mol
Formula C₉H₁₂BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in constructing pyrimidine-based scaffolds found in bioactive molecules. Commonly utilized in medicinal chemistry for modifying core structures to enhance potency and selectivity. Also employed in the preparation of antiviral and anticancer agents through cross-coupling and nucleophilic substitution reactions. Its protected amine group allows for selective functionalization, making it valuable in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,194.50
inventory 100mg
10-20 days ฿5,439.50
inventory 250mg
10-20 days ฿9,619.50

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tert-Butyl (2-bromopyrimidin-5-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in constructing pyrimidine-based scaffolds found in bioactive molecules. Commonly utilized in medicinal chemistry for modifying core structures to enhance potency and selectivity. Also employed in the preparation of antiviral and anticancer agents through cross-coupling and nucleophilic substitution reactions. Its protected amine group allows for selective functi

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It plays a key role in constructing pyrimidine-based scaffolds found in bioactive molecules. Commonly utilized in medicinal chemistry for modifying core structures to enhance potency and selectivity. Also employed in the preparation of antiviral and anticancer agents through cross-coupling and nucleophilic substitution reactions. Its protected amine group allows for selective functionalization, making it valuable in multi-step organic syntheses.

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