5-Chloro-N3-ethylpyridazine-3, 4-diamine

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Reagent Code: #164019
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CAS Number 1614246-24-0

science Other reagents with same CAS 1614246-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.62 g/mol
Formula C₆H₉ClN₄
badge Registry Numbers
MDL Number MFCD30471056
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

description Product Description

Used as an 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 explored in agrochemical research for designing novel pesticides with improved selectivity and lower environmental impact. Its chloro and amine functional groups allow for easy modification, enabling rapid derivatization in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,090.00
inventory 100mg
10-20 days ฿3,710.00
inventory 250mg
10-20 days ฿8,530.00

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5-Chloro-N3-ethylpyridazine-3, 4-diamine
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Used as an 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 explored in agrochemical research for designing novel pesticides with improved selectivity and lower environmental impact. Its chloro and amine functional groups allow for easy mod

Used as an 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 explored in agrochemical research for designing novel pesticides with improved selectivity and lower environmental impact. Its chloro and amine functional groups allow for easy modification, enabling rapid derivatization in drug discovery programs.

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