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2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97%

2,2':5',2
849062-17-5
CAS-Nr.
849062-17-5
Englisch Name:
2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97%
Synonyma:
2,2':5',2"-Terthiophene-5-boronic acid pinacol ester 96%;2-(5’,2-Bithiophen-2’-yl)thiophene-5-boronic acid,pinacol;2,2':5',2\\-Terthiophene-5-boronic acid pinacol ester 96%";2-([2,2':5',2''-Terthiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-([2,2':5',2''-Terthiophen]-5-yl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[2,2':5',2''-terthiophen]-5-yl-;4,4,5,5-tetramethyl-2-[5-(5-thiophen-2-ylthiophen-2-yl)thiophen-2-yl]-1,3,2-dioxaborolane
CBNumber:
CB2972464
Summenformel:
C18H19BO2S3
Molgewicht:
374.35
MOL-Datei:
849062-17-5.mol

2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97% Eigenschaften

Schmelzpunkt:
109-113 °C(lit.)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature

Sicherheit

WGK Germany  3

2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97% Chemische Eigenschaften,Einsatz,Produktion Methoden

2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97% Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2,2':5',2"-Terthiophene-5-boronic acid pinacol ester, 97% Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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  • 2-(5’,2-Bithiophen-2’-yl)thiophene-5-boronic acid,pinacol
  • 2-([2,2':5',2''-Terthiophen]-5-yl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
  • 2,2':5',2"-Terthiophene-5-boronic acid pinacol ester 96%
  • 4,4,5,5-tetramethyl-2-[5-(5-thiophen-2-ylthiophen-2-yl)thiophen-2-yl]-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[2,2':5',2''-terthiophen]-5-yl-
  • 2,2':5',2\\-Terthiophene-5-boronic acid pinacol ester 96%"
  • 2-([2,2':5',2''-Terthiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 849062-17-5
  • C18H19BO2S3
  • Boronate Esters
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Heteroaryl Boronate Esters
  • Materials Science
  • Organic and Printed Electronics
  • Organometallic Reagents
  • Synthetic Tools and Reagents
  • Thiophene Monomers and Building Blocks
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