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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sorrisi canonici | CN1C2=C(C(=O)N(C1=O)C)N(C=N2)CCCNC3COC4C3OCC4O[N+](=O)[O-] |
|---|---|
| IUPAC Name | [(3S,3aR,6S,6aS)-3-[3-(1,3-dimethyl-2,6-dioxopurin-7-yl)propylamino]-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-6-yl] nitrate |
| InChIKey | XTEGRRHNMFDROI-YRRQLQLVSA-N |
| INCHI | 1S/C16H22N6O7/c1-19-14-11(15(23)20(2)16(19)24)21(8-18-14)5-3-4-17-9-6-27-13-10(29-22(25)26)7-28-12(9)13/h8-10,12-13,17H,3-7H2,1-2H3/t9-,10-,12+,13+/m0/s1 |
| Isomeri SMILES | CN1C2=C(C(=O)N(C1=O)C)N(C=N2)CCCN[C@H]3CO[C@H]4[C@@H]3OC[C@@H]4O[N+](=O)[O-] |
| CAS alternativo | 81792-35-0 |
| PubChem CID | 3034007 |
| Termini MeSH | KC 046;KC-046;teopranitol |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Classe | Imidazopyrimidines |
| Subclass | Purines and purine derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Xanthines |
| Alternative Parents | 6-oxopurines Alkaloids and derivatives Furofurans Pyrimidones N-substituted imidazoles Vinylogous amides Oxolanes Alkyl nitrates Heteroaromatic compounds Ureas Organic nitro compounds Organic nitric acids and derivatives Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Dialkylamines Organic oxides Organic salts Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Xanthine - 6-oxopurine - Purinone - Alkaloid or derivatives - Furofuran - Pyrimidone - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Organic nitrate - Oxolane - Heteroaromatic compound - Vinylogous amide - Alkyl nitrate - Urea - Organic nitro compound - Organic nitric acid or derivatives - Lactam - Azacycle - Secondary amine - Oxacycle - Dialkyl ether - Ether - Secondary aliphatic amine - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Amine - Organic oxygen compound - Organonitrogen compound - Organic salt - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety. |
| External Descriptors | Not available |
| Peso molecolare | 410.380 g/mol |
|---|---|
| XLogP3 | -0.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 6 |
| Exact Mass | 410.155 Da |
| Monoisotopic Mass | 410.155 Da |
| Topological Polar Surface Area | 144.000 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 675.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 |