![]() | |
Names | |
---|---|
Preferred IUPAC name
(1s,3s,5s)-Cyclohexane-1,3,5-triamine | |
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).
|
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.
It is prepared from the tris carbamate of cyclohexane. The latter is generated via the Curtius rearrangement starting from cyclohexanetricarboxylic acid. [1]
![]() | |
Names | |
---|---|
Preferred IUPAC name
(1s,3s,5s)-Cyclohexane-1,3,5-triamine | |
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).
|
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.
It is prepared from the tris carbamate of cyclohexane. The latter is generated via the Curtius rearrangement starting from cyclohexanetricarboxylic acid. [1]