cis,cis-1,3,5-Triaminocyclohexane
cis,cis-1,3,5-Triaminocyclohexane is an organic compound with the formula (CH2CHNH2)3. It is a triamine. Of the many isomers possible for triaminocyclohexane, the cis,cis-1,3,5-derivative has attracted attention because it is a common tripodal ligand, abbreviated as tach. It is a colorless oil. It is a popular tridentate ligand in coordination chemistry.
Names | |
---|---|
IUPAC name
(1s,3s,5s)-1,3,5-Cyclohexanetriamine | |
Other names
TACH; cis,cis-Cyclohexane-1,3,5-triamine | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
PubChem CID |
|
| |
| |
Properties | |
C6H15N3 | |
Molar mass | 129.207 g·mol−1 |
Appearance | Colorless liquid |
Boiling point | 285 °C (545 °F; 558 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
It is prepared from the triscarbamate of cyclohexane. The latter is generated via the Curtius rearrangement starting from cyclohexanetricarboxylic acid.[1]
References
- Bowen, Tom; Planalp, Roy P.; Brechbiel, Martin W. (1996). "An improved synthesis of cis,cis-1,3,5-triaminocyclohexane. Synthesis of novel hexadentate ligand derivatives for the preparation of gallium radiopharmaceuticals". Bioorganic & Medicinal Chemistry Letters. 6 (7): 807–810. doi:10.1016/0960-894X(96)00110-2.
- Schwarzenbach, Gerold; Bürgi, Hans-Beat; Jensen, William P.; Lawrance, Geoffrey A.; Mønsted, Lene; Sargeson, Alan M. (1983). "Acid Cleavage of Nickel(Ii) Complexes Containing cis,cis-1,3,5-Cyclohexanetriamine (TACH), Crystal Structure of [Ni(tach)(H2O)3](NO3)2, and a Correlation Between the Structure and Reactivity of Nickel-Polyamine Complexes". Inorganic Chemistry. 22 (26): 4029–4038. doi:10.1021/ic00168a042.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.