(2-Chloro-6-methoxypyridin-4-yl)methanamine dihydrochloride

95%

Reagent Code: #131549
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CAS Number 2703756-89-0

science Other reagents with same CAS 2703756-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.53 g/mol
Formula C₇H₁₁Cl₃N₂O
badge Registry Numbers
MDL Number MFCD34187008
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing active pharmaceutical ingredients (APIs) due to its reactivity and stability in multi-step reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,700.00
inventory 250mg
10-20 days ฿28,000.00

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(2-Chloro-6-methoxypyridin-4-yl)methanamine dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing active pharmaceutical ingredients (APIs) due to its reactivity and stability in multi-step reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing active pharmaceutical ingredients (APIs) due to its reactivity and stability in multi-step reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.
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