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2,3-THIOPHENEDICARBOXALDEHYDE

2,3-THIOPHENEDICARBOXALDEHYDE Struktur
932-41-2
CAS-Nr.
932-41-2
Englisch Name:
2,3-THIOPHENEDICARBOXALDEHYDE
Synonyma:
BUTTPARK 154\50-98;TIMTEC-BB SBB004162;2,3-DiforMylthiophene;2,3-Thiophenedialdehyde;2,3-ThiophenedicarboxaL;2,3-THIOPHENEDICARBOXYLATE;THIOPHENE-2,3-DICARBALDEHYDE;2,3-Thiophene-dicarbaldehyde;2,3-Dicarbaldehyde thiophene;2,3-THIOPHENEDICARBOXALDEHYDE
CBNumber:
CB4694067
Summenformel:
C6H4O2S
Molgewicht:
140.16
MOL-Datei:
932-41-2.mol

2,3-THIOPHENEDICARBOXALDEHYDE Eigenschaften

Schmelzpunkt:
76-78 °C (lit.)
Siedepunkt:
134 °C / 22mmHg
Dichte
1.370±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
L?slichkeit
soluble in Methanol
Aggregatzustand
powder to crystal
Farbe
White to Light yellow
CAS Datenbank
932-41-2(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  3
HS Code  2934999090
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
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

2,3-THIOPHENEDICARBOXALDEHYDE Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

brown powder

Verwenden

2,3-Thiophenedicarboxaldehyde may be employed for the synthesis of TIPSE (triisopropylsilylethynyl)-substituted dibromoanthradithiophene (TIPSEBr2- AntDT).

Allgemeine Beschreibung

2,3-Thiophenedicarboxaldehyde undergoes aldol reaction with (4aS,9R,9aR,10S)-11-(propan-2-ylidene)-2,3,4a,9,9a,10-hexahydro-9,10-methanoanthracene-1,4-dione under oxygen-free conditions affords (5aS,6S,11R,11aR)-14-(propan-2-ylidene)-5a,6,11,11a-tetrahydro-6,11-methanotetraceno[3,2-b]thiophene-5,12-dione.

2,3-THIOPHENEDICARBOXALDEHYDE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2,3-THIOPHENEDICARBOXALDEHYDE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 183)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652
info@fdachem.com China 20287 58
Springchem New Material Technology Co.,Limited
+86-021-62885108 +8613917661608
info@spring-chem.com China 2068 57
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29791 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886
info@dakenam.com China 18781 58
AB PharmaTech,LLC
323-480-4688
sales@acrospharmatech.com United States 989 55
Shandong chuangyingchemical Co., Ltd.
18853181302
sale@chuangyingchem.com CHINA 5906 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873
sales@chemdad.com China 39894 58
Alchem Pharmtech,Inc.
8485655694
sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49374 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29811 58

932-41-2()Verwandte Suche:


  • BUTTPARK 154\50-98
  • THIOPHENE-2,3-DICARBALDEHYDE
  • THIOPHENE-2,3-DICARBOXALDEHYDE
  • TIMTEC-BB SBB004162
  • 2,3-THIOPHENEDICARBOXYLATE
  • 2,3-THIOPHENEDICARBOXALDEHYDE
  • 2,3-Dicarbaldehyde thiophene
  • 2,3-Thiophenedialdehyde
  • Thiophene 2,3-dicarboxyaldehyde
  • 2,3-Thiophene-dicarbaldehyde
  • 2,3-DiforMylthiophene
  • 2,3-Thiophenedicarboxaldehyde 97%
  • 2,3-ThiophenedicarboxaL
  • 2,3-Thiophenedicarboxaldehyde (7CI, 8CI, 9CI, ACI)
  • 2,3-Bisthiophenecarboxaldehyde
  • 932-41-2
  • 983-41-2
  • Building Blocks
  • Thiophenes
  • Heterocyclic Building Blocks
  • Thiophene Series
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiophenes
  • Heterocyclic Compounds
  • Functional Materials
  • Reagents for Conducting Polymer Research
  • Thiophene Derivatives (for Conduting Polymer Research)
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