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CAS 21436-03-3

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(+)-trans-1,2-Diaminocyclohexane

Description:
(+)-trans-1,2-Diaminocyclohexane, with the CAS number 21436-03-3, is an organic compound characterized by its cyclic structure and the presence of two amino groups (-NH2) attached to a cyclohexane ring. This compound is a chiral molecule, existing in two enantiomeric forms, with the (+) designation indicating the specific optical activity of the trans isomer. The trans configuration refers to the spatial arrangement of the amino groups, which are positioned on opposite sides of the cyclohexane ring, influencing its steric and electronic properties. This compound is often utilized in coordination chemistry and as a ligand in metal complexes due to its ability to form stable chelates. Additionally, it has potential applications in pharmaceuticals and materials science, where its unique structural features can impart specific functionalities. The presence of the amino groups also allows for hydrogen bonding, which can affect solubility and reactivity in various chemical environments. Overall, (+)-trans-1,2-Diaminocyclohexane is a versatile compound with significant implications in both theoretical and applied chemistry.
Formula:C6H14N2
InChI:InChI=1S/C6H14N2/c7-5-3-1-2-4-6(5)8/h5-6H,1-4,7-8H2/t5-,6-/m0/s1
InChI key:InChIKey=SSJXIUAHEKJCMH-WDSKDSINSA-N
SMILES:N[C@@H]1[C@@H](N)CCCC1
Synonyms:
  • ((1S,2S)-2-Aminocyclohexyl)amine
  • (+)-(S,S)-1,2-Diaminocyclohexane
  • (+)-(S,S)-Dach
  • (+)-trans-1,2-Cyclohexanediamine
  • (+)-trans-1,2-Diaminocyclohexane
  • (1S,2S)-(+)-1,2-Aminocyclohexane
  • (1S,2S)-(+)-1,2-Cyclohexanediamine
  • (1S,2S)-(+)-Diaminocyclohexane
  • (1S,2S)-(+)-trans-1,2-Diaminocyclohexane
  • (1S,2S)-1,2-trans-Cyclohexanediamine
  • See more synonyms
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