Triazinane

Last updated
Triazinane
Triazinane isomerism.png
Identifiers
3D model (JSmol)
8477997
ChEBI
ChemSpider
PubChem CID
  • 1,2,3:InChI=1S/C3H9N3/c1-2-4-6-5-3-1/h4-6H,1-3H2
    Key: OYWRDHBGMCXGFY-UHFFFAOYSA-N
  • 1,2,4:InChI=1S/C3H9N3/c1-2-5-6-3-4-1/h4-6H,1-3H2
    Key: VWKKSBDTNICZRS-UHFFFAOYSA-N
  • 1,3,5:InChI=1S/C3H9N3/c1-4-2-6-3-5-1/h4-6H,1-3H2
    Key: LKLLNYWECKEQIB-UHFFFAOYSA-N
  • 1,2,3:C1CNNNC1
  • 1,2,4:C1CNNCN1
  • 1,3,5:C1NCNCN1
Properties
C3H9N3
Molar mass 87.126 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Triazinanes are a class of nitrogen-containing heterocycles. [1] Triazinanes have six-membered cyclohexane-like ring but with three carbon centers replaced by nitrogen. The parent have the molecular formula (CH2)3(NH)3. Three isomeric forms are possible, but only 1,3,5-triazinanes are common. 1,3,5-triazinane is a labile intermediate in the formation of hexamethylenetetramine from ammonia and formaldehyde.

Stable 1,3,5-Triorganotriazines are formed by condensation of primary amines and formaldehyde. [2]

See also

References

  1. ↑ Heterocyclic Chemistry T.L. Gilchrist 1985 ISBN   0-582-01421-2 (1997, ISBN   0-582-27843-0
  2. ↑ Nielsen, Arnold T.; Atkins, Ronald L.; Moore, Donald W.; Scott, Robert; Mallory, Daniel; LaBerge, Jeanne M. (1973). "Structure and chemistry of the aldehyde ammonias. 1-Amino-1-alkanols, 2,4,6-trialkyl-1,3,5-hexahydrotriazines, and N,N-dialkylidene-1,1-diaminoalkanes". J. Org. Chem. 38 (19): 3288–3295. doi:10.1021/jo00959a010.
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