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Merck
모든 사진(2)

주요 문서

모든 문서 보기

747157

Sigma-Aldrich

Potassium pentafluroroethyltrifluoroborate

95%

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C2BF8K
CAS Number:
476639-90-4
Molecular Weight:
225.92
MDL number:
MFCD17214187
UNSPSC 코드:
12352103
PubChem Substance ID:
329765814
NACRES:
NA.22

Quality Level

100

분석

95%

양식

solid

mp

252-257 °C

작용기

fluoro

저장 온도

2-8°C

SMILES string

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

InChI

1S/C2BF8.K/c4-1(5,2(6,7)8)3(9,10)11;/q-1;+1

InChI key

PSJPJAFBTMLFFX-UHFFFAOYSA-N

애플리케이션

Organotrifluoroborate involved in:
  • Suzuki Miyaura cross-coupling reactions, and polymerization reactions
  • Synthesis of photonic crystals
  • Synthesis of sensitizers for dye-sensitized solar cells
  • Mannich / diastereoselective hydroamination reaction sequence

Organotrifluoroborates as versatile and stable boronic acid surrogates

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCT0081
MKBV0943V
MKBT7229V
MKBQ3517V

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문서 라이브러리 방문

S. Achelle;
Journal of Polymer Science: Part A, General Papers, 48, 2659-2665 (2010)
Emilio Alacid et al.
The Journal of organic chemistry, 74(6), 2321-2327 (2009-02-17)
Potassium vinyl and alkenyltrifluoroborates are cross-coupled with aryl and heteroaryl bromides using 1 mol % Pd loading of 4-hydroxyacetophenone oxime derived palladacycle or Pd(OAc)2 as precatalysts, K2CO3 as base, and TBAB as additive and water reflux under conventional or microwave
Jenny M Baxter Vu et al.
Organic letters, 13(15), 4056-4059 (2011-07-14)
A new two-step synthesis of highly substituted pyrrolidines has been developed. Chiral silane Lewis acid promoted enantioselective Mannich reactions of silyl ketene imines with acylhydrazones may be used to access bishomoallylic benzoic hydrazides that in turn may be cyclized to
Gary A Molander et al.
Journal of the American Chemical Society, 130(47), 15792-15793 (2008-11-05)
A method was developed for the hydroboration of alkenyl-containing organotrifluoroborates to generate dibora intermediates. The reactivity differences between organotrifluoroborates and trialkylboranes facilitated the cross-coupling of the borane moiety of these intermediates in a highly chemoselective fashion with aryl halides, leaving
R. Grisorio;
Journal of Polymer Science: Part A, General Papers, 49, 842-847 (2011)
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