| Weight | 150.253 g/mol |
|---|---|
| Formula | C2H2N2S3 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Xanthane hydride (6846-35-1)
3-amino-1,2,4-dithiazole-5-thione
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- Large-Scale Synthesis of Oligonucleotide Phosphorothioates Using 3-Amino-1,2,4-dithiazole-5-thione as an Efficient Sulfur-Transfer Reagent (Organic Process Research & Development, 2000)
- Rates of formation of isoperthiocyanic acid (5-Amino-1,2,4-dithiazole-3-thione) from thiocyanate in aqueous solution (Australian Journal of Chemistry, 1969)
- The crystal structure of xanthane hydride (Acta Crystallographica, 1963)
- Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1,2,4-dithiazole-5-thione (xanthane hydride) (Organic and Biomolecular Chemistry, 2007)
- The crystal structure of di(5-amino-3-thione-1,2,4-dithiazole)tris-thiocyanatobismuthate(III), (C2H2N2S3)2Bi(SCN)3 (Zeitschrift Fur Kristallographie, 1989)
- 5-Amino-3H-1,2,4-dithiazole-3-thione as a synthon: New synthesis of 2-thioureidobenzheteroazoles (Heteroatom Chemistry, 1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-amino-1,2,4-dithiazole-5-thione
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SMILESC1(=NC(=S)SS1)N
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InChIKeyYWZHEXZIISFIDA-UHFFFAOYSA-N
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Xanthane hydride
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