Ethyl 2, 2-Difluoro-2-(4-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)phenyl)acetate

98%

Reagent Code: #184886
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CAS Number 1683545-35-8

science Other reagents with same CAS 1683545-35-8

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Weight 326.14 g/mol
Formula C₁₆H₂₁BF₂O₄
badge Registry Numbers
MDL Number MFCD20278276
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated organic compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The difluoroacetate moiety allows for the introduction of fluorine atoms, which can enhance metabolic stability and lipophilicity in drug candidates. Commonly applied in the development of bioactive molecules and functional materials requiring tailored electronic or steric properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,370.00
inventory 250mg
10-20 days ฿3,370.00
inventory 1g
10-20 days ฿11,090.00

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Ethyl 2, 2-Difluoro-2-(4-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)phenyl)acetate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated organic compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The difluoroacetate moiety allows for the introduction of fluorine atoms, which can enhance metabolic stability and lipophilicity in drug candidates. Commonly applied in the development of bioactive molecules and functional materials requiring tailor

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated organic compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The difluoroacetate moiety allows for the introduction of fluorine atoms, which can enhance metabolic stability and lipophilicity in drug candidates. Commonly applied in the development of bioactive molecules and functional materials requiring tailored electronic or steric properties.

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