| Weight | 150.232 g/mol |
|---|---|
| Formula | C2H6N4S2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2,5-DITHIOBIUREA (142-46-1)
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- TCI - 2,5-DITHIOBIUREA24.00 - 46.00 USD
- New bifunctional N-thiophosphorylated thiourea and 2,5-dithiobiurea derivatives. Crystal structures of R[C(S)NHP(S)(OiPr)2]2 (R = N(Ph)CH2CH2N(Ph) and NHNH) (Polyhedron, 2008)
- Supramolecular coordination complexes of the N-thiophosphorylated 2,5-dithiobiurea [NHC(S)NHP(S-(OiPr)2]2 with Zn(II) and Cd(II): Cation induced dinuclear mesocate structure versus tetranuclear nanoscaled aggregate (European Journal of Inorganic Chemistry, 2014)
- The influence of the spacer Z on N-phosphorylated bis-thioureas and 2,5-dithiobiurea Z[C(S)NHP(O)(OiPr)2]2 (Z = NHCH2CH2NH, NHC6H4-2-NH, NHNH) crystal design (Polyhedron, 2009)
- Diorganotin(IV) complexes of 2,5dithiobiurea (H2dtbu). The crystal structures of Me2Sn(dtbu) and Ph2Sn(dtbu) (Heteroatom Chemistry, 2006)
- Reactions of Dimethyl Acetylenedicarboxylate with 2,5-Dithiobiurea Derivatives (Synthesis, 2014)
- Studies on Thiosemicarbazide Derivatives. III: 1-Acyl-2, 5-dithiobiurea@@@1-Acyl-2,5-dithiobiurea (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1958)
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SMILESC(=S)(N)NNC(=S)N
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InChIKeyKCOYHFNCTWXETP-UHFFFAOYSA-N
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2,5-DITHIOBIUREA
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