3-(2,2,2-Trifluoroethoxy)anilinehydrochloride

95%

Reagent Code: #244413
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CAS Number 1049756-13-9

science Other reagents with same CAS 1049756-13-9

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Weight 227.61 g/mol
Formula C₈H₉ClF₃NO
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoroethoxy group contributes to improved lipophilicity and resistance to oxidative degradation, making it valuable in medicinal chemistry. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and central nervous system agents. Also utilized in agrochemical research for designing novel pesticides and herbicides where fluorine substitution enhances activity and environmental persistence. Suitable for coupling reactions in heterocyclic synthesis due to the aromatic amine functionality.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,020.00
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3-(2,2,2-Trifluoroethoxy)anilinehydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoroethoxy group contributes to improved lipophilicity and resistance to oxidative degradation, making it valuable in medicinal chemistry. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and central nervous system agents. Also utilized in agrochemical research for designing novel pesti

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its trifluoroethoxy group contributes to improved lipophilicity and resistance to oxidative degradation, making it valuable in medicinal chemistry. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and central nervous system agents. Also utilized in agrochemical research for designing novel pesticides and herbicides where fluorine substitution enhances activity and environmental persistence. Suitable for coupling reactions in heterocyclic synthesis due to the aromatic amine functionality.

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