(CDU-NHC-01)3-(4-Methyl-2,6-bis((R)-1-phenylethyl)phenyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazol-3-ium tetrafluoroborate
≥98%
Reagent
Code: #157498
CAS Number
2828444-06-8
blur_circular Chemical Specifications
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Molecular Information
Weight
539.48 g/mol
Formula
C₃₁H₃₄BF₄NS
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Storage & Handling
Storage
2-8°C, light-proof, inert gas
description Product Description
Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis, enabling highly enantioselective transformations such as C–C bond formations and hydrogenations. Its sterically tuned, chiral environment makes it effective in transition metal complexes for catalyzing reactions with high stereocontrol, particularly in pharmaceutical and fine chemical synthesis where optical purity is critical. Also employed in organocatalytic systems for ring-opening, cycloaddition, and desymmetrization reactions.
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(CDU-NHC-01)3-(4-Methyl-2,6-bis((R)-1-phenylethyl)phenyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazol-3-ium tetrafluoroborate
Used as a chiral N-heterocyclic carbene (NHC) precursor in asymmetric catalysis, enabling highly enantioselective transformations such as C–C bond formations and hydrogenations. Its sterically tuned, chiral environment makes it effective in transition metal complexes for catalyzing reactions with high stereocontrol, particularly in pharmaceutical and fine chemical synthesis where optical purity is critical. Also employed in organocatalytic systems for ring-opening, cycloaddition, and desymmetrization reactions.
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