Telluropyrylium information

Telluropyrylium
Names
	Preferred IUPAC name Telluropyrylium
	Other names Tellurinium; Tellurapyrylium
Identifiers
CAS Number	84030-84-2;
3D model (JSmol)	Interactive image;
ChemSpider	26667642;
	InChI InChI=1S/C5H5Te/c1-2-4-6-5-3-1/h1-5H/q+1 Key: MAFRBFVUOYFWCN-UHFFFAOYSA-N;
	SMILES C1=CC=[Te+]C=C1;
Properties
Chemical formula	C5H5Te+
Molar mass	192.69 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Telluropyrylium is an aromatic heterocyclic compound consisting of a six member ring with five carbon atoms, and a positively charged tellurium atom.^[2]^[3] Derivatives of telluropyrylium are important in research of infrared dyes.^[4]

^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1097. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
^ Doddi, Giancarlo; Ercolani, Gianfranco (1994). "Thiopyrylium, Selenopyrylium, and Telluropyrylium Salts". Advances in Heterocyclic Chemistry Volume 60. Vol. 60. pp. 65–195. doi:10.1016/S0065-2725(08)60182-8. ISBN 9780120207602.
^ Sugimoto, Toyonari (1981). "Reactions of Pyrylium, Thiopyrylium and Selenopyrylium Salts and Their Application to Synthetic Utility". Journal of Synthetic Organic Chemistry, Japan. 39 (1): 1–13. doi:10.5059/yukigoseikyokaishi.39.1.
^ Detty, Michael R.; O'regan, Marie B. (1994). "Telluropyrylium Compounds". Chemistry of Heterocyclic Compounds: Tellurium-Containing Heterocycles. Chemistry of Heterocyclic Compounds: A Series of Monographs. Wiley. pp. 219–289. doi:10.1002/9780470187937.ch4. ISBN 9780470187937.

[1] International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1097. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.

[doddi-2] Doddi, Giancarlo; Ercolani, Gianfranco (1994). "Thiopyrylium, Selenopyrylium, and Telluropyrylium Salts". Advances in Heterocyclic Chemistry Volume 60. Vol. 60. pp. 65–195. doi:10.1016/S0065-2725(08)60182-8. ISBN 9780120207602.

[sugimoto-3] Sugimoto, Toyonari (1981). "Reactions of Pyrylium, Thiopyrylium and Selenopyrylium Salts and Their Application to Synthetic Utility". Journal of Synthetic Organic Chemistry, Japan. 39 (1): 1–13. doi:10.5059/yukigoseikyokaishi.39.1.

[4] Detty, Michael R.; O'regan, Marie B. (1994). "Telluropyrylium Compounds". Chemistry of Heterocyclic Compounds: Tellurium-Containing Heterocycles. Chemistry of Heterocyclic Compounds: A Series of Monographs. Wiley. pp. 219–289. doi:10.1002/9780470187937.ch4. ISBN 9780470187937.

Telluropyrylium information

and 15 Related for: Telluropyrylium information

Telluropyrylium

Boratabenzene

Pyrylium

Phosphorine

Borabenzene

Benzene

Heterocyclic compound

Germabenzene

Pyridine

Thiopyrylium

Arsabenzene

Stannabenzene

Selenopyrylium

Stibinin

Silabenzene

Names

Preferred IUPAC name Telluropyrylium^[1]
Other names Tellurinium; Tellurapyrylium
Identifiers
CAS Number	84030-84-2
3D model (JSmol)	Interactive image
ChemSpider	26667642
InChI InChI=1S/C5H5Te/c1-2-4-6-5-3-1/h1-5H/q+1 Key: MAFRBFVUOYFWCN-UHFFFAOYSA-N
SMILES C1=CC=[Te+]C=C1
Properties
Chemical formula	C₅H₅Te⁺
Molar mass	192.69 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references