potassium trifluoro-[2-(hydroxymethyl)phenyl]boranuide

98%

Reagent Code: #226152
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CAS Number 850623-74-4

science Other reagents with same CAS 850623-74-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.0344 g/mol
Formula C₇H₇BF₃KO
badge Registry Numbers
MDL Number MFCD04115769
thermostat Physical Properties
Melting Point 300℃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boron-based structure facilitates mild and selective transformations, making it valuable in pharmaceutical and agrochemical manufacturing. The presence of a hydroxymethyl group enhances solubility and can direct regioselectivity in coupling processes. Suitable for constructing biaryl compounds and complex aromatic systems under palladium catalysis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,100.00
inventory 5g
10-20 days ฿17,900.00

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potassium trifluoro-[2-(hydroxymethyl)phenyl]boranuide
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Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boron-based structure facilitates mild and selective transformations, making it valuable in pharmaceutical and agrochemical manufacturing. The presence of a hydroxymethyl group enhances solubility and can direct regioselectivity in coupling processes. Suitable for constructing biaryl compounds and complex aromatic systems under palladium catalysis.

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boron-based structure facilitates mild and selective transformations, making it valuable in pharmaceutical and agrochemical manufacturing. The presence of a hydroxymethyl group enhances solubility and can direct regioselectivity in coupling processes. Suitable for constructing biaryl compounds and complex aromatic systems under palladium catalysis.

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