3-(2,2-Difluoroethoxy)pyridine-2-carboxylic acid

95%

Reagent Code: #178116
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CAS Number 1250216-31-9

science Other reagents with same CAS 1250216-31-9

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scatter_plot Molecular Information
Weight 203.14 g/mol
Formula C₈H₇F₂NO₃
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MDL Number MFCD14653080
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its pyridine structure with a 2-carboxylic acid and 3-(2,2-difluoroethoxy) substitution enables effective binding in biologically active molecules, enhancing metabolic stability and target selectivity. The carboxylic acid group facilitates subsequent reactions such as amide or ester formation, while the difluoroethoxy moiety improves cell membrane permeability. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates. Also utilized in agrochemicals for designing novel pesticides due to its favorable electronic and steric properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,050.00
inventory 100mg
10-20 days ฿8,570.00
inventory 250mg
10-20 days ฿15,320.00
inventory 1g
10-20 days ฿48,260.00

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3-(2,2-Difluoroethoxy)pyridine-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its pyridine structure with a 2-carboxylic acid and 3-(2,2-difluoroethoxy) substitution enables effective binding in biologically active molecules, enhancing metabolic stability and target selectivity. The carboxylic acid group facilitates subsequent reactions such as amide or ester formation, while the difluoroethoxy moiety improves cell membrane permeability. C

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antiviral drugs. Its pyridine structure with a 2-carboxylic acid and 3-(2,2-difluoroethoxy) substitution enables effective binding in biologically active molecules, enhancing metabolic stability and target selectivity. The carboxylic acid group facilitates subsequent reactions such as amide or ester formation, while the difluoroethoxy moiety improves cell membrane permeability. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates. Also utilized in agrochemicals for designing novel pesticides due to its favorable electronic and steric properties.

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