7-(Trifluoromethyl)imidazo[1,2-a]pyrimidine

≥97%

Reagent Code: #173512
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CAS Number 375857-66-2

science Other reagents with same CAS 375857-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.12 g/mol
Formula C₇H₄F₃N₃
badge Registry Numbers
MDL Number MFCD08234997
inventory_2 Storage & Handling
Storage Room temperature, 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. Shows utility in medicinal chemistry for constructing bioactive molecules due to its ability to enhance metabolic stability and binding affinity. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and capacity to cross the blood-brain barrier. Commonly found in research settings for optimizing lead compounds in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,570.00
inventory 5g
10-20 days ฿6,740.00
inventory 25g
10-20 days ฿21,770.00

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7-(Trifluoromethyl)imidazo[1,2-a]pyrimidine
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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. Shows utility in medicinal chemistry for constructing bioactive molecules due to its ability to enhance metabolic stability and binding affinity. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and capacity to cross the blood-brain barrier. Commonly found in research settings for optimizing lead compounds in

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for constructing bioactive molecules due to its ability to enhance metabolic stability and binding affinity. Also employed in the design of CNS-active compounds owing to its favorable physicochemical properties and capacity to cross the blood-brain barrier. Commonly found in research settings for optimizing lead compounds in drug discovery programs.

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