3-Thenoesure
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- CAS-Nr.
- 88-13-1
- Bezeichnung:
- 3-Thenoesure
- Englisch Name:
- 3-Thiophenezoic acid
- Synonyma:
- THIOPHENE-3-CARBOXYLIC ACID;3-THIOPHENECARBOXYLIC ACID;3-THENOIC ACID;3-Thenoylic acid;3-Thiophenecarboxylic;Thiophene-3-carboxylic acid ,99%;S0503;AKOS 207-06;AKOS B013976;JACS-88-13-1
- CBNumber:
- CB6141040
- Summenformel:
- C5H4O2S
- Molgewicht:
- 128.15
- MOL-Datei:
- 88-13-1.mol
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3-Thenoesure Eigenschaften
- Schmelzpunkt:
- 136-141 °C (lit.)
- Siedepunkt:
- 260°C (estimate)
- Dichte
- 1.305 (estimate)
- Brechungsindex
- 1.5160 (estimate)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- L?slichkeit
- water: soluble0.2g/10 mL, clear to almost clear, colorless to slightly brownish-yellow
- Aggregatzustand
- Crystalline Powder
- pka
- 4.1(at 25℃)
- Farbe
- White to slightly yellow
- Wasserl?slichkeit
- 4.3 g/L (25 ºC)
- Merck
- 14,9279
- BRN
- 1994
- InChI
- InChI=1S/C5H4O2S/c6-5(7)4-1-2-8-3-4/h1-3H,(H,6,7)
- InChIKey
- YNVOMSDITJMNET-UHFFFAOYSA-N
- SMILES
- C1SC=CC=1C(O)=O
- CAS Datenbank
- 88-13-1(CAS DataBase Reference)
3-Thenoesure Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-S?tze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Beschreibung
3-Thiophenezoic acid is a polymer monomer that can be used to synthesise thiophene derivative polymers, such as the poly(3-thiophene benzoic acid) (PTPA), the copolymer of 3-bromothiophene (BTP) and 3-thiophenezoic acid (TPA). These compounds are an important class of conductive polymers, typically exhibiting favourable electrochemical activity, environmental stability, and ease of processing.
Chemische Eigenschaften
white to light yellow crystal powder
Verwenden
3-Thiophenecarboxylic Acid was used as a lading compound for the development of a clinic useful D-amino acid inhibitor and have the potential to sever as active site proves to elucidate the structure-function relationships of D-amino acids.
Allgemeine Beschreibung
Mechanism of photopolymerization of 3-thiophenecarboxylic acid catalyzed by potassium dichromate has been reported.
3-Thenoesure Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
3-Thenoesure Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 451)Lieferanten
88-13-1(3-Thenoesure)Verwandte Suche:
- 3-Carboxythiophene
- 3-Thiophenecarboxylic acid,99%
- 3-Carboxythiophene, 3-Thenoic acid
- 3-Thiophenecarboxylic acid, 99% 1GR
- 3-Thiophenecarboxylic Acid
3-Thiophenic Acid
- 3 - thiophene forMic acid
- 3-Thiophenearboxylic acid
- THIOPHEN-3-CARBOCYLIC ACID
- 3-THIOPHENEFORMIC ACID 98+%
- 3-Thiophenecarboxylic acid 99%
- AKOS B013976
- AKOS 207-06
- 3-Thiophenezoic acid
- 3-THIOPHENIC ACID
- 3-Thiophenoic acid
- Thiophene-3-carboxylic acid≥ 98% (HPLC)
- Thiophene-3-carboxylic acid for synthesis
- BETA-THIOPHENIC ACID
- B-THIOPHENIC ACID
- ART-CHEM-BB B013976
- RARECHEM AL BO 0765
- TIMTEC-BB SBB004240
- 3-thienylcarboxylicacid
- beta-thiophenecarboxylicacid
- Thiophene-3-carboxylic acid 98%
- Thiophene-3-carboxylic acid, 98.5%
- JACS-88-13-1
- 3-Thenoesure
- 3-ThiophenecarboxyL
- Thiophene-3-formic acid
- 3-Thiophenezoic acid ISO 9001：2015 REACH
- S0503
- Thiophene-3-carboxylic acid ,99%
- 3-Thenoylic acid
- 3-THENOIC ACID
- 3-Thiophenecarboxylic acid (6CI, 7CI, 8CI, 9CI, ACI)
- Thiophen-3-carboxylic acid
- 3-Thiophenecarboxylic
- 3-THIOPHENECARBOXYLIC ACID
- THIOPHENE-3-CARBOXYLIC ACID
- 88-13-1
- 99-13-1
- 1006-40-6
- C5H4O2S
- Thiophene Derivatives (for Conduting Polymer Research)
- Building Blocks
- Heterocyclic Building Blocks
- Thiophenes
- Reagents for Conducting Polymer Research
- Thiophene&Benzothiophene
- Organic acids
- Heterocyclic Compounds
- Functional Materials
- Reagents for Conducting Polymer Research
- Thiophene Derivatives (for Conduting Polymer Research)
- Thiophen
- Thiophens
- Building Blocks
