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About This Item
經驗公式（希爾表示法）:
C6H3BF3KN2O
CAS號碼:
分子量：:
226.01
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22
推薦產品
化驗
96%
形狀
solid
mp
>300 °C
SMILES 字串
[K+].F[B-](F)(F)c1ccc2nonc2c1
InChI
1S/C6H3BF3N2O.K/c8-7(9,10)4-1-2-5-6(3-4)12-13-11-5;/h1-3H;/q-1;+1
InChI 密鑰
VVXGHNBCIPLVLI-UHFFFAOYSA-N
應用
Organotrifluoroborate invovled in copper-mediated cross-coupling and Suzuki cross-coupling
Organotrifluoroborates as versatile and stable boronic acid surrogates.
Organotrifluoroborates as versatile and stable boronic acid surrogates.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Synthesis of 5-aryl- and 5-heteroaryl-7-carboxyl-8-hydroxyquinaldines through Suzuki cross-coupling reaction with potassium organotrifluoroborates
F. Sliman and D. Desmaele,
Synthesis, 4, 619-630 (2010)
Sebastian A Testero et al.
Bioorganic & medicinal chemistry letters, 21(9), 2675-2678 (2011-01-25)
The copper-mediated and non-basic oxidative cross-coupling of organotrifluoroborates with phenols was applied to elaboration of the structures of thiirane-based inhibitors of matrix metalloproteinases. By revision of the synthetic sequence to allow this cross-coupling as the final step, and taking advantage
文章
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
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