5-Bromo-N-(trans-4-hydroxycyclohexyl)-2-pyridinecarboxamide

95%

Reagent Code: #49066
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CAS Number 1279028-26-0

science Other reagents with same CAS 1279028-26-0

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Weight 299.1637 g/mol
Formula C₁₂H₁₅BrN₂O₂
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases. Its structural features make it suitable for designing inhibitors that can modulate enzyme activity, which is crucial in treating diseases like cancer, inflammation, and neurodegenerative disorders. Additionally, its bromo and hydroxy groups provide reactive sites for further chemical modifications, enabling the creation of diverse derivatives for screening and optimization in pharmacological research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,592.00
inventory 1g
10-20 days ฿27,792.00
inventory 100mg
10-20 days ฿6,948.00

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5-Bromo-N-(trans-4-hydroxycyclohexyl)-2-pyridinecarboxamide
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases. Its structural features make it suitable for designing inhibitors that can modulate enzyme activity, which is crucial in treating diseases like cancer, inflammation, and neurodegenerative disorders. Additionally, its bromo and hydroxy groups provide reactive sites for further chemical

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases. Its structural features make it suitable for designing inhibitors that can modulate enzyme activity, which is crucial in treating diseases like cancer, inflammation, and neurodegenerative disorders. Additionally, its bromo and hydroxy groups provide reactive sites for further chemical modifications, enabling the creation of diverse derivatives for screening and optimization in pharmacological research.

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