2-bromo-N4-methylpyridine-3,4-diamine

≥95%

Reagent Code: #216932
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CAS Number 1396554-44-1

science Other reagents with same CAS 1396554-44-1

blur_circular Chemical Specifications

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Weight 202.05 g/mol
Formula C₆H₈BrN₃
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MDL Number MFCD22415287
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Also employed in research settings to design new drug candidates targeting inflammatory diseases and neurological disorders. Shows utility in agrochemical research for developing novel pesticides with improved selectivity. Commonly used in cross-coupling reactions to build complex heterocyclic systems in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,050.00
inventory 250mg
10-20 days ฿13,100.00

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2-bromo-N4-methylpyridine-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. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Also employed in research settings to design new drug candidates targeting inflammatory diseases and neurological disorders. Shows utility in agrochemical research for developing novel pesticides with improved selectivity. Commonly used in cross-couplin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Also employed in research settings to design new drug candidates targeting inflammatory diseases and neurological disorders. Shows utility in agrochemical research for developing novel pesticides with improved selectivity. Commonly used in cross-coupling reactions to build complex heterocyclic systems in medicinal chemistry.

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