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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Kanonisches Lächeln | C1NCNC(=S)N1 |
|---|---|
| IUPAC Name | 1,3,5-triazinane-2-thione |
| InChIKey | HBEQQDRAYMGDPU-UHFFFAOYSA-N |
| INCHI | 1S/C3H7N3S/c7-3-5-1-4-2-6-3/h4H,1-2H2,(H2,5,6,7) |
| Isomere SMILES | C1NCNC(=S)N1 |
| PubChem CID | 1897601 |
| Molekulargewicht | 117.18 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Klasse | Triazinanes |
| Subclass | 1,3,5-triazinanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 1,3,5-triazinanes |
| Alternative Parents | Thioureas Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | 1,3,5-triazinane - Thiourea - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as 1,3,5-triazinanes. These are triazinanes having three nitrogen ring atoms at the 1-, 3-, and 5- positions. |
| External Descriptors | Not available |
| Molekulargewicht | 117.180 g/mol |
|---|---|
| XLogP3 | -0.500 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 117.036 Da |
| Monoisotopic Mass | 117.036 Da |
| Topological Polar Surface Area | 68.200 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 74.200 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |