2-(3-cyanophenyl)-2,2-difluoroacetic acid

74%

Reagent Code: #162282
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CAS Number 1249974-01-3

science Other reagents with same CAS 1249974-01-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.14 g/mol
Formula C₉H₅F₂NO₂
thermostat Physical Properties
Boiling Point 334.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.42±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability. Its difluoroacetic acid moiety contributes to improved lipophilicity and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its ability to mimic carboxylic acid groups while offering greater resistance to enzymatic degradation. Also utilized in agrochemical research for designing novel pesticides with increased environmental persistence and target specificity.

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Test Parameter Specification
Appearance White solid
Purity (%) 74-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,220.00
inventory 1g
10-20 days ฿13,500.00

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2-(3-cyanophenyl)-2,2-difluoroacetic acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability. Its difluoroacetic acid moiety contributes to improved lipophilicity and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its ability to mimic carboxylic acid groups while offering greater resistance to enzymatic degradation. Also utilized in agrochemical research

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability. Its difluoroacetic acid moiety contributes to improved lipophilicity and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its ability to mimic carboxylic acid groups while offering greater resistance to enzymatic degradation. Also utilized in agrochemical research for designing novel pesticides with increased environmental persistence and target specificity.

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