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Merck

711101

Sigma-Aldrich

吡啶-3-三氟硼酸钾

97%

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About This Item

经验公式(希尔记法):
C5H4BF3KN
分子量:
185.00
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

powder

mp

228-232 °C

SMILES 字串

[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 密鑰

MNCKCIOWIHHCSC-UHFFFAOYSA-N

相关类别

應用

An organotrifluoroborate involved in:
  • 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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

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


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分析证书(COA)

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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.

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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