Ethyl-(5-fluoro-pyrimidin-2-yl)-amine

97%

Reagent Code: #185019
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CAS Number 1289386-10-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 141.15 g/mol
Formula C₆H₈FN₃
badge Registry Numbers
MDL Number MFCD18837174
thermostat Physical Properties
Boiling Point 234 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.216 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing targeted therapies. Also employed in agrochemical research for creating novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its fluorinated heteroaromatic core, which enhances metabolic stability and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿27,150.00
Ethyl-(5-fluoro-pyrimidin-2-yl)-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing targeted therapies. Also employed in agrochemical research for creating novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its fluorinated heteroaromatic core, which enhances metabolic s

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing targeted therapies. Also employed in agrochemical research for creating novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its fluorinated heteroaromatic core, which enhances metabolic stability and bioavailability in drug candidates.

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