2,4-BIS(TRIFLUOROMETHYL)PHENYL-TRIFLUOROBORATE POTASSIUM SALT

98%

Reagent Code: #148060
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CAS Number 1150655-10-9

science Other reagents with same CAS 1150655-10-9

blur_circular Chemical Specifications

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Weight 320 g/mol
Formula C₈H₃BF₉K
badge Registry Numbers
MDL Number MFCD07368252
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The presence of trifluoromethyl groups enhances lipophilicity and metabolic stability in target molecules, making this reagent valuable in designing bioactive compounds. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,660.00
inventory 5g
10-20 days ฿7,510.00

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2,4-BIS(TRIFLUOROMETHYL)PHENYL-TRIFLUOROBORATE POTASSIUM SALT
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Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The presence of trifluoromethyl groups enhances lipophilicity and metabolic stability in target molecules, making this reagent valuable in designing bioactive compounds. It is particularly useful in late-stage

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The presence of trifluoromethyl groups enhances lipophilicity and metabolic stability in target molecules, making this reagent valuable in designing bioactive compounds. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups under mild reaction conditions.

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