δ-2:2'-Bis(1,3-dithiazol)
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- CAS-Nr.
- 31366-25-3
- Bezeichnung:
- δ-2:2'-Bis(1,3-dithiazol)
- Englisch Name:
- TETRATHIAFULVALENE
- Synonyma:
- TTF;ARHH;RHOH;NSC 222862;etrathiafulvalene;TETRATHIAFULVALENE;Tetrathiafulvalene 97%;Tetrathiafulvalene,98%;Tetrathiafulvalene,97%;ω-2,2’-Bi-1,3-dithiole
- CBNumber:
- CB6359496
- Summenformel:
- C6H4S4
- Molgewicht:
- 204.34
- MOL-Datei:
- 31366-25-3.mol
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δ-2:2'-Bis(1,3-dithiazol) Eigenschaften
- Schmelzpunkt:
- 116-119 °C (lit.)
- Siedepunkt:
- 90℃ (1 Torr)
- Dichte
- 1.448 (estimate)
- Brechungsindex
- 1.6000 (estimate)
- storage temp.
- 2-8°C
- Aggregatzustand
- Crystals or Crystalline Powder
- Farbe
- Orange to brownish
- Wasserl?slichkeit
- It is insoluble in water. Soluble in organic solvents.
- Sensitive
- Air & Light Sensitive
- maximale Wellenl?nge (λmax)
- 369nm(CHCl3)(lit.)
- Merck
- 14,9242
- BRN
- 1617956
- InChIKey
- FHCPAXDKURNIOZ-UHFFFAOYSA-N
- CAS Datenbank
- 31366-25-3(CAS DataBase Reference)
- EPA chemische Informationen
- 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)- (31366-25-3)
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
Bildanzeige (GHS) |
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Alarmwort |
Warnung |
Gefahrenhinweise |
Code |
Gefahrenhinweise |
Gefahrenklasse |
Abteilung |
Alarmwort |
Symbol |
P-Code |
H317 |
Kann allergische Hautreaktionen verursachen. |
Sensibilisierung der Haut |
Kategorie 1A |
Warnung |
src="/GHS07.jpg" width="20" height="20" /> |
P261, P272, P280, P302+P352,P333+P313, P321, P363, P501 |
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Sicherheit |
P261 |
Einatmen von Staub vermeiden. |
P321 |
Besondere Behandlung |
P333+P313 |
Bei Hautreizung oder -ausschlag: ?rztlichen Rat einholen/?rztliche Hilfe hinzuziehen. |
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δ-2:2'-Bis(1,3-dithiazol) Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R43:Sensibilisierung durch Hautkontakt m?glich.
S-S?tze Betriebsanweisung:
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
Chemische Eigenschaften
ORANGE TO BROWNISH CRYSTALS OR CRYSTALLINE POWDER
Verwenden
Tetrathiafulvalene, holds wide application in HPLC, NMR. This heterocyclic compound contributed to the development of molecular electronics. They are used as a organic super conductors.
Allgemeine Beschreibung
Tetrathiafulvalene (TTF) is an electron-donor which consists of oligomers, dendrimers and polymers which can be used in the formation of redox macromolecules.
l?uterung methode
Recrystallise it from cyclohexane/hexane under an argon atmosphere [Kauzlarich et al. J Am Chem Soc 109 4561 1987]. [Beilstein 19/11 V 380.]
δ-2:2'-Bis(1,3-dithiazol) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
δ-2:2'-Bis(1,3-dithiazol) Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 144)Lieferanten
31366-25-3(δ-2:2'-Bis(1,3-dithiazol))Verwandte Suche:
- 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)-
- 1,4,5,8-Tetrathiafulvalen
- 1,4,5,8-Tetrathiafulvalene
- 2-(1,3-dithiol-2-ylidene)-1,3-dithiol
- Δ2,2μ-Bi-1,3-dithiole, TTF
- Delta2,2'-bi-1,3-dithiol
- [2,2']-Bi[1,3]-dithioylidene
- Tetrathiafulvalene, 99+% 1GR
- Tetrathiafulvalene, 99+% 250MG
- Anti-RHOH, C-Terminal antibody produced in rabbit
- ARHH
- GTP-binding protein TTF
- RHOH
- Rho-related GTP-binding protein RhoH
- Tetrathiafulvalene (purified by sublimation)
- NSC 222862
- Tetrathiafulvalene 97%
- 2,2'-bi(1,3-dithiolylidene)
- DELTA2,2'-BI-1,3-DITHIOLE
- DELTA^2^,^2^-Bi-1,3-dithiole~TTF
- delta-2:2-bis(1,3-dithiazole)
- TetrathiafulvaleneTTForangextl
- Tetrathiafulvalene,98%
- Tetrathiafulvalene,97%
- Tetrathiafulvalene, 99+%
- 2-(1,3-Dithiol-2-ylidene)-1,3-dithiole
- 2-(1,3-dithiol-2-ylidene)-3-dithiole
- ω-2,2’-Bi-1,3-dithiole
- Tetrathiafulvalene,98+%TTF
- TETRATHIAFULVALENE TTF
- TETRATHIAFULVALENE
- TTF
- Tetrathiafulvalene, 98.5%
- etrathiafulvalene
- tetrathiafulvalene dication
- 2,2'-Bi(1,3-dithiolylidene)
- 31366-25-3
- C6H4S4
- Heterocyclic Building Blocks
- Others
- S-Containing
- Building Blocks
- Donors (Charge Transfer Complexes)
- TTF Derivatives
- Charge Transfer Complexes for Organic Metals
- Functional Materials
- TTF Derivatives
- Building Blocks
- Chemical Synthesis
- Heterocyclic Building Blocks
- Materials Science
- Organic and Printed Electronics
- Organic Field Effect Transistor (OFET) Materials
- Others
- p-Type Organic Semiconductors
- p-Type Small Molecules
- S-Containing
- Charge Transfer Complexes for Organic Metals