2.2.2-Cryptand
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Names | |||
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Systematic IUPAC name
4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane[1] | |||
Other names
Cryptating agent 222 | |||
Identifiers | |||
3D model (JSmol) |
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Abbreviations | Crypt-222 | ||
620282 | |||
ChemSpider | |||
ECHA InfoCard | 100.041.770 | ||
EC Number | 245-962-4 | ||
MeSH | Cryptating+agent+222 | ||
PubChem CID |
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RTECS number | MP4750000 | ||
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Properties | |||
C 18N 2H 36O 6 | |||
Molar mass | 376.4882 g mol−1 | ||
Melting point | 68 to 71 °C (154 to 160 °F; 341 to 344 K) | ||
Hazards | |||
GHS pictograms | |||
GHS signal word | WARNING | ||
H315, H319, H335 | |||
P261, P305+351+338 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
2.2.2-Cryptand is one of the most important members of the cryptand family of chelating agents. In Nomenclature of Inorganic Chemistry (2005), IUPAC recommends the abbreviation "crypt-222".
References
- ↑ "cryptating agent 222 - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information. Descriptors Computed from Structure.
- ↑ Alberto, R.; Ortner, K.; Wheatley, N.; Schibli, R.; Schubiger, A. P. (2001). "Synthesis and properties of boranocarbonate: a convenient in situ CO source for the aqueous preparation of [99mTc(OH2)3(CO)3]+". J. Am. Chem. Soc. 121 (13): 3135–3136. doi:10.1021/ja003932b.
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