2-ethynyl-5-(trifluoromethyl)pyridine

≥95%

Reagent Code: #181988
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CAS Number 379670-42-5

science Other reagents with same CAS 379670-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.12 g/mol
Formula C₈H₄F₃N
badge Registry Numbers
MDL Number MFCD13189717
inventory_2 Storage & Handling
Storage 2-8°C, 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 medicinal chemistry. Also employed in agrochemicals to enhance the efficacy of crop protection agents. The trifluoromethyl group improves metabolic stability, while the ethynyl moiety enables further functionalization through coupling reactions. Widely utilized in research for building complex heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,120.00
inventory 1g
10-20 days ฿29,780.00
inventory 100mg
10-20 days ฿5,960.00

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2-ethynyl-5-(trifluoromethyl)pyridine
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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 medicinal chemistry. Also employed in agrochemicals to enhance the efficacy of crop protection agents. The trifluoromethyl group improves metabolic stability, while the ethynyl moiety enables further functionalization through coupling reactions. Widely utilized in research for buil

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 medicinal chemistry. Also employed in agrochemicals to enhance the efficacy of crop protection agents. The trifluoromethyl group improves metabolic stability, while the ethynyl moiety enables further functionalization through coupling reactions. Widely utilized in research for building complex heterocyclic compounds.

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