U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C3H3N3S3
Molecular Weight 177.271
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3,5-TRIAZINANE-2,4,6-TRITHIONE

SMILES

S=C1NC(=S)NC(=S)N1

InChI

InChIKey=WZRRRFSJFQTGGB-UHFFFAOYSA-N
InChI=1S/C3H3N3S3/c7-1-4-2(8)6-3(9)5-1/h(H3,4,5,6,7,8,9)

HIDE SMILES / InChI

Molecular Formula C3H3N3S3
Molecular Weight 177.271
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Tris(methylammonium thiocyanurate) monohydrate.
2010-12-08
Tripropyl-ammonium trithio-cyanurate.
2010-10-13
Design and synthesis of a stable supramolecular trigonal prism formed by the self-assembly of a linear tetrakis(Zn2+-cyclen) complex and trianionic trithiocyanuric acid in aqueous solution and its complexation with DNA (cyclen = 1,4,7,10-tetraazacyclododecane).
2009-10-05
A hydrogen-bonded channel structure formed by a complex of uracil and melamine.
2007-05-23
Heavy metal removal from winery wastewater in the case of restrictive discharge regulation.
2007
Coordination polymers of copper(I) halides and neutral heterocyclic thiones with new coordination modes.
2005-05-30
Structural rationalisation of co-crystals formed between trithiocyanuric acid and molecules containing hydrogen bonding functionality.
2005-04-08
UV-Induced trithione --> trithiol triple proton transfer in trithiocyanuric acid isolated in low-temperature matrixes.
2005-03-17
Synthesis, structure, redox, NLO and DNA interaction aspects of [((L'-'")2RuII)3(mu3-L)]3+ and [(L')2RuII(NC5H4S-)]+[L3- = 1,3,5-triazine-2,4,6-trithiolato, L'-'" = arylazopyridine].
2004-06-07
[Supramolecular chemistry of multinuclear zinc(II) complexes in aqueous solution].
2002-12
[Creation of new supramolecular chemistry based on multiple interaction in aqueous solution].
2002-10
Effectiveness of commercial reagents for heavy metal removal from water with new insights for future chelate designs.
2002-05-27
A cuboctahedral supramolecular capsule by 4:4 self-assembly of Tris(Zn(II)-cyclen) and trianionic trithiocyanurate in aqueous solution at neutral pH (cyclen=1,4,7,10-tetraazacyclododecane).
2002-02-15
Aqueous leaching properties and environmental implications of cadmium, lead and zinc trimercaptotriazine (TMT) compounds.
2001-10
Chemistry of 2,4,6-trimercapto-1,3,5-triazine (TMT): acid dissociation constants and group 2 complexes.
2001-08-13
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.
1994-08-17
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:31:33 GMT 2025
Edited
by admin
on Mon Mar 31 22:31:33 GMT 2025
Record UNII
KX0WZE0QAQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-62071
Preferred Name English
1,3,5-TRIAZINANE-2,4,6-TRITHIONE
Systematic Name English
2,4,6-TRITHIO-5-AZAURACIL
Systematic Name English
CYANURIC ACID, TRITHIO-
Systematic Name English
2,4,6-TRIMERCAPTO-1,3,5-TRIAZINE
Systematic Name English
S-TRIAZINE-2,4,6-TRITHIOL
Systematic Name English
NSC-65480
Code English
2,4,6-TRIAZINETRITHIOL
Systematic Name English
2,4,6-TRIMERCAPTO-S-TRIAZINE
Systematic Name English
2,4,6-TRITHIOL-1,3,5-TRIAZINE
Systematic Name English
1,3,5-TRIMERCAPTOTRIAZINE
Systematic Name English
S-TRIAZINE-2,4,6(1H,3H,5H)-TRITHIONE
Systematic Name English
1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRITHIONE
Systematic Name English
1,3,5-TRIAZINE-2,4,6-TRITHIOL
Systematic Name English
2,4,6-TRIMERCAPTOTRIAZINE
Systematic Name English
Code System Code Type Description
CAS
638-16-4
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-322-8
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
NSC
62071
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
NSC
65480
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
FDA UNII
KX0WZE0QAQ
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID3045067
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY
PUBCHEM
1268121
Created by admin on Mon Mar 31 22:31:33 GMT 2025 , Edited by admin on Mon Mar 31 22:31:33 GMT 2025
PRIMARY