2-(3,5-Difluorophenyl)ethanoylchloride

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Reagent Code: #132503
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CAS Number 157033-24-4

science Other reagents with same CAS 157033-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.57 g/mol
Formula C₈H₅ClF₂O
badge Registry Numbers
MDL Number MFCD00275597
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its acyl chloride functionality allows for efficient amide and ester bond formation, making it valuable in constructing active pharmaceutical ingredients (APIs). Commonly employed in the preparation of kinase inhibitors and other biologically active molecules where the difluorophenyl group contributes to target binding affinity. Also utilized in agrochemical synthesis for creating novel herbicides and pesticides with improved environmental persistence and efficacy. Its reactivity enables rapid derivatization in medicinal chemistry research, especially in late-stage functionalization of complex molecules.

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inventory 25g
10-20 days ฿24,010.00

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2-(3,5-Difluorophenyl)ethanoylchloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its acyl chloride functionality allows for efficient amide and ester bond formation, making it valuable in constructing active pharmaceutical ingredients (APIs). Commonly employed in the preparation of kinase inhibitors and other biologically active molecules where the difluorophenyl group contributes to target bindi

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its acyl chloride functionality allows for efficient amide and ester bond formation, making it valuable in constructing active pharmaceutical ingredients (APIs). Commonly employed in the preparation of kinase inhibitors and other biologically active molecules where the difluorophenyl group contributes to target binding affinity. Also utilized in agrochemical synthesis for creating novel herbicides and pesticides with improved environmental persistence and efficacy. Its reactivity enables rapid derivatization in medicinal chemistry research, especially in late-stage functionalization of complex molecules.

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