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2,2'-BITHIOPHENE-5-CARBOXALDEHYDE

2,2'-BITHIOPHENE-5-CARBOXALDEHYDE Struktur
3779-27-9
CAS-Nr.
3779-27-9
Englisch Name:
2,2'-BITHIOPHENE-5-CARBOXALDEHYDE
Synonyma:
S1180;AKOS BAR-0540;BUTTPARK 29\08-48;TIMTEC-BB SBB003601;SALOR-INT L158844-1EA;5-FORMYL-2,2'-BITHIOPHENE;2,2'-BITHIOPHENE-5-CARBALDEHYDE;2,2'-BITHIENYL-5-CARBOXALDEHYDE;2,2'-Bithiophene-5-carboxaldehy;2,2'-BITHIOPHENE-5-CARBOXALDEHYDE
CBNumber:
CB1105713
Summenformel:
C9H6OS2
Molgewicht:
194.27
MOL-Datei:
3779-27-9.mol
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2,2'-BITHIOPHENE-5-CARBOXALDEHYDE Eigenschaften

Schmelzpunkt:
55-58 °C(lit.)
Siedepunkt:
210 °C / 18mmHg
Dichte
1.424 g/cm3
Flammpunkt:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
Aggregatzustand
powder to crystal
Farbe
White to Amber to Dark green
CAS Datenbank
3779-27-9(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
S-Sätze: 24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29349990
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P271 Nur im Freien oder in gut belüfteten Räumen verwenden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

2,2'-BITHIOPHENE-5-CARBOXALDEHYDE Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

yellow-brown to brown crystalline powder

Verwenden

2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following:
  • boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process
  • (2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with 4-nitrophenylhydrazine
  • bithiophene fulleropyrrolidine obtained via refluxing with sarcosine and fullerene
  • azomethine phthalic diimides by heating with N,N-bis(4-amino-2,3,5,6-tetramethylphenyl)naphthalene-1,4,5,8-dicarboximide (DANDI)

Synthesis Reference(s)

Synthetic Communications, 19, p. 307, 1989 DOI: 10.1080/00397918908050983

2,2'-BITHIOPHENE-5-CARBOXALDEHYDE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

2,2'-Bithiophen N,N-Dimethylformamid Phosphorylchlorid

Downstream Produkte

5-BROMO-2,2'-BITHIOPHENE-5'-CARBOXALDEHYDE 2-(2,2'-bithiophen-5-ylmethylene)malononitrile

2,2'-BITHIOPHENE-5-CARBOXALDEHYDE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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3779-27-9()Verwandte Suche:

2,2'-Bithiophen
  • BUTTPARK 29\08-48
  • 5-FORMYL-2,2'-BITHIOPHENE
  • 5-(THIEN-2-YL)-2-THIOPHENECARBALDEHYDE
  • AKOS BAR-0540
  • 2,2''-BITHIENYL-5-CARBOXALDEHYDE 98%
  • 2,2'-BITHIOPHENE-5-CARBOXALDEHYDE
  • 2,2'-BITHIENYL-5-CARBOXALDEHYDE
  • 2,2'-BITHIOPHENE-5-CARBALDEHYDE
  • TIMTEC-BB SBB003601
  • SALOR-INT L158844-1EA
  • 2,2'-Bithienyl-5-carboxaldehyde,98%
  • 2,2zzhlxy-Bithiophene-5-carboxaldehyde
  • 2,2'-Bithiophene-5-carboxaldehyde,5-ForMyl-2,2'-bithiophene
  • 2,2'-Bithiophene-5-carboxaldehyde 98%
  • 5-thiophen-2-yl-2-thiophenecarboxaldehyde
  • 2,2'-Bithiophene-5-carboxaldehy
  • 2,2'-Bithiophene-5-carboxaldehyde>
  • S1180
  • 2,2''-Biothiophene-5-carboxaldehyde
  • 2,2'-Bithiophene]-5-carboxaldehyde
  • 3779-27-9
  • C9H6OS2
  • ALDEHYDE
  • Thiophenes
  • Heterocyclic Building Blocks
  • Reagents for Conducting Polymer Research
  • Thiophene Derivatives (for Conduting Polymer Research)
  • Building Blocks
  • Thiophene Derivatives (for Conduting Polymer Research)
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiophenes
  • Heterocyclic Compounds
  • Functional Materials
  • Reagents for Conducting Polymer Research
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