5-(3-methylphenyl)pyridin-2-amine

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Reagent Code: #210311
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CAS Number 893738-40-4

science Other reagents with same CAS 893738-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.24 g/mol
Formula C₁₂H₁₂N₂
badge Registry Numbers
MDL Number MFCD06802146
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of selective receptor modulators for neurological disorders. Its structural features make it valuable in optimizing drug potency and metabolic stability during lead compound development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,080.00

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5-(3-methylphenyl)pyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of selective receptor modulators for neurological disorders. Its structural features make it valuable in optimizing drug potency and metabolic stabil

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of selective receptor modulators for neurological disorders. Its structural features make it valuable in optimizing drug potency and metabolic stability during lead compound development.

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