Potassium trifluoro[(2-fluorophenyl)methyl]boranuide

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Reagent Code: #227515
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CAS Number 1246073-48-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BF₄K
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral reducing agent in asymmetric synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It facilitates the selective reduction of prochiral ketones and imines, enabling efficient synthesis of active pharmaceutical ingredients (APIs) with high optical purity. Its stability and selectivity make it suitable for use in late-stage transformations where functional group tolerance is critical. Also employed in research settings for developing new synthetic routes in medicinal chemistry and fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿2,660.00
Potassium trifluoro[(2-fluorophenyl)methyl]boranuide
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Used as a chiral reducing agent in asymmetric synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It facilitates the selective reduction of prochiral ketones and imines, enabling efficient synthesis of active pharmaceutical ingredients (APIs) with high optical purity. Its stability and selectivity make it suitable for use in late-stage transformations where functional group tolerance is critical. Also employed in research settings for developing n

Used as a chiral reducing agent in asymmetric synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It facilitates the selective reduction of prochiral ketones and imines, enabling efficient synthesis of active pharmaceutical ingredients (APIs) with high optical purity. Its stability and selectivity make it suitable for use in late-stage transformations where functional group tolerance is critical. Also employed in research settings for developing new synthetic routes in medicinal chemistry and fine chemical manufacturing.

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