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![Potassium trifluoro[(pyrrolidin-1-yl)methyl]borate AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/603/307/0f7c53df-8fc7-4d09-bc76-d55556863e97/640/0f7c53df-8fc7-4d09-bc76-d55556863e97.png)
Quality Level
assay
97%
form
powder
mp
228-232 °C
SMILES string
[K+].F[B-](F)(F)c1cccnc1
InChI
1S/C5H4BF3N.K/c7-6(8,9)5-2-1-3-10-4-5;/h1-4H;/q-1;+1
InChI key
MNCKCIOWIHHCSC-UHFFFAOYSA-N
Related Categories
Application
- Nickel-catalyzed cross-coupling reactions and C-O activation
- Suzuki cross-coupling
- Copper-catalyzed cross-coupling reactions
- Stereoselective Mukaiyama aldol reactions
Organotrifluoroborates as versatile and stable boronic acid surrogates.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Articles
These bench stable Potassium Organotrifluoroborates are useful for Suzuki-Miyaura cross-coupling reactions and have also been used for a variety of other C-C bond forming reactions. Importantly, these reagents are compatible with a wide range of functional groups and are stable to many commonly used and harsh reaction conditions.
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