Quinoxalin-6-yl-methylamine hydrochloride

≥95%

Reagent Code: #228439
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CAS Number 1276056-88-2

science Other reagents with same CAS 1276056-88-2

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Weight 195.65 g/mol
Formula C₉H₉N₃·HCl
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MDL Number MFCD15424795
inventory_2 Storage & Handling
Storage Room temperature

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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting cancer and infectious diseases. Also employed in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,090.00
inventory 250mg
10-20 days ฿6,170.00
inventory 1g
10-20 days ฿15,460.00
inventory 5g
10-20 days ฿58,960.00

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Quinoxalin-6-yl-methylamine hydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting cancer and infectious diseases. Also employed in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly utilized in medicinal chemistry for sca

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting cancer and infectious diseases. Also employed in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly utilized in medicinal chemistry for scaffold modification to improve pharmacokinetic properties.

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