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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline

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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline Basic information

Product Name:
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline
Synonyms:
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline 97%
  • 6-(tetraMethyl-1,3,2-dioxaborolan-2-yl)quinoxaline
  • 2-dioxaborolan-2-yl)quinoxaline
  • Quinoxaline-6-boronic acid picol ester
  • Quinoxaline, 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:
1167418-13-4
MF:
C14H17BN2O2
MW:
256.11
Mol File:
1167418-13-4.mol
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline Chemical Properties

Boiling point:
387.8±22.0 °C(Predicted)
Density 
1.123 g/mL at 25℃
refractive index 
n20/D1.560
Flash point:
>110℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
0.93±0.30(Predicted)
InChIKey
ZYWICCYXTGRUNM-UHFFFAOYSA-N
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
2933998090
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline Usage And Synthesis

Uses

Quinoxaline-6-boronic acid pinacol ester is a common reactant of a Suzuki coupling reaction that can be used:

  • To prepare quinoxalin based PI3Kδ inhibitors.
  • As a substrate in the Cu(II) catalyzed [11C]-radiocyanation of arylboronic acids.
  • To prepare 6-quinoxaline boronic acid, which is used as a substrate in the silver-mediated fluorination of boronic acids.

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxalineSupplier

Zhuhai Aobokai Biomedical Technology Co., Ltd. Gold
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400-0628126 15697568815;
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J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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BeiJing Hwrk Chemicals Limted
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0757-86329057 18934348241
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Energy Chemical
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Bellen Chemistry Co., Ltd.
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010-60400361
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info@bellenchem.com
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline(1167418-13-4)Related Product Information