(6-methoxypyridin-3-yl)methanamine hydrochloride

97%

Reagent Code: #210307
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CAS Number 857220-13-4

science Other reagents with same CAS 857220-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.63 g/mol
Formula C₇H₁₁ClN₂O
badge Registry Numbers
MDL Number MFCD08061344
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine group and aromatic structure, which facilitate coupling reactions in drug design. Commonly employed in research settings for the creation of novel compounds targeting neurological disorders and inflammatory diseases. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions and purification processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,790.00
1g
10-20 days ฿4,900.00
5g
10-20 days ฿17,990.00
(6-methoxypyridin-3-yl)methanamine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine group and aromatic structure, which facilitate coupling reactions in drug design. Commonly employed in research settings for the creation of novel compounds targeting neurological disorders and inflammatory diseases. Its hydrochloride salt form enhanc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine group and aromatic structure, which facilitate coupling reactions in drug design. Commonly employed in research settings for the creation of novel compounds targeting neurological disorders and inflammatory diseases. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction conditions and purification processes.

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