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Merck

659274

Sigma-Aldrich

烯丙基三氟硼酸钾

95%

别名:

Potassium trifluoro(prop-2-enyl)borate

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About This Item

经验公式(希尔记法):
C3H5BF3K
分子量:
147.98
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

95%

形狀

solid

mp

>300 °C

SMILES 字串

[K+].F[B-](F)(F)CC=C

InChI

1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2H,1,3H2;/q-1;+1

InChI 密鑰

TVPZAMJXLCDMIT-UHFFFAOYSA-N

相关类别

應用

Organotrifluoroborate involved in:
  • Catalytic allylboration
  • Stereoselective nucleophilic addition
  • Pd-catalyzed heterocyclizations
  • Oxidation reactions and Oxidative Mannich reactions
  • Cross-coupling reactions

Organotrifluoroborates as versatile and stable boronic acid surrogates.

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - 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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

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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