5-(tert-Butyl)pyridin-3-amine hydrochloride

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Reagent Code: #124358
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CAS Number 2135331-65-4

science Other reagents with same CAS 2135331-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.68 g/mol
Formula C₉H₁₅ClN₂
badge Registry Numbers
MDL Number MFCD31556146
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a building block for the development of more complex chemical structures, particularly in pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Its tert-butyl and pyridine amine groups make it a versatile reagent for creating compounds with specific binding properties. Additionally, it is employed in the preparation of ligands for catalysis, aiding in the development of efficient catalytic systems for chemical transformations. Its hydrochloride form enhances solubility, making it easier to handle in aqueous or polar solvent-based reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,107.00
inventory 250mg
10-20 days ฿28,647.00

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5-(tert-Butyl)pyridin-3-amine hydrochloride
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This compound is primarily utilized in organic synthesis as a building block for the development of more complex chemical structures, particularly in pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Its tert-butyl and pyridine amine groups make it a versatile reagent for creating compounds with specific binding properties. Additionally, it is employed in the prep

This compound is primarily utilized in organic synthesis as a building block for the development of more complex chemical structures, particularly in pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Its tert-butyl and pyridine amine groups make it a versatile reagent for creating compounds with specific binding properties. Additionally, it is employed in the preparation of ligands for catalysis, aiding in the development of efficient catalytic systems for chemical transformations. Its hydrochloride form enhances solubility, making it easier to handle in aqueous or polar solvent-based reactions.

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