Methyl 1-(2,2,2-trifluoroethyl)-1H-pyrazole-3-carboxylate

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Reagent Code: #39121
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CAS Number 1245772-13-7

science Other reagents with same CAS 1245772-13-7

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Weight 208.1379 g/mol
Formula C₇H₇F₃N₂O₂
badge Registry Numbers
MDL Number MFCD18262321
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description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoroethyl group and a pyrazole ring, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of active ingredients for drugs targeting neurological disorders, inflammation, and metabolic diseases. Additionally, its trifluoroethyl group can enhance the metabolic stability and bioavailability of the final compounds. In agrochemical research, it serves as a building block for creating pesticides and herbicides with improved efficacy and selectivity. Its versatility and unique chemical properties make it a key component in advanced research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,671.00

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Methyl 1-(2,2,2-trifluoroethyl)-1H-pyrazole-3-carboxylate
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This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoroethyl group and a pyrazole ring, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of active ingredients for drugs targeting neurological disorders, inflammation, and metabolic diseases. Additionally, its trifluoroethyl group can enhance the m

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoroethyl group and a pyrazole ring, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of active ingredients for drugs targeting neurological disorders, inflammation, and metabolic diseases. Additionally, its trifluoroethyl group can enhance the metabolic stability and bioavailability of the final compounds. In agrochemical research, it serves as a building block for creating pesticides and herbicides with improved efficacy and selectivity. Its versatility and unique chemical properties make it a key component in advanced research and industrial applications.

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