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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Kanonisches Lächeln | C1COP(=O)(OC1C2=CC(=CC=C2)Cl)COCCN3C=NC4=C(N=CN=C43)N |
|---|---|
| IUPAC Name | 9-[2-[[(2R,4S)-4-(3-chlorophenyl)-2-oxo-1,3,2\u03bb5-dioxaphosphinan-2-yl]methoxy]ethyl]purin-6-amine |
| InChIKey | GWNHAOBXDGOXRR-HJFSHJIFSA-N |
| INCHI | 1S/C17H19ClN5O4P/c18-13-3-1-2-12(8-13)14-4-6-26-28(24,27-14)11-25-7-5-23-10-22-15-16(19)20-9-21-17(15)23/h1-3,8-10,14H,4-7,11H2,(H2,19,20,21)/t14-,28+/m0/s1 |
| Isomere SMILES | C1CO[P@@](=O)(O[C@@H]1C2=CC(=CC=C2)Cl)COCCN3C=NC4=C(N=CN=C43)N |
| Alternative CAS-Nummer | 625095-60-5 |
| PubChem CID | 9604654 |
| MeSH-Eintrag | hepavir-B;ICN 2001-3;ICN-2001-3;ICN2001-3;MB 06866;MB-06866;MB-6866;MB06866;pradefovir;pradefovir mesylate;remofovir;remofovir mesylate |
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Klasse | Imidazopyrimidines |
| Subclass | Purines and purine derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 6-aminopurines |
| Alternative Parents | Aminopyrimidines and derivatives Chlorobenzenes Dialkyl alkylphosphonates Aryl chlorides Phosphonic acid esters Imidolactams N-substituted imidazoles Heteroaromatic compounds Azacyclic compounds Oxacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Organochlorides Organooxygen compounds Organophosphorus compounds Organopnictogen compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 6-aminopurine - Halobenzene - Phosphonic acid diester - Chlorobenzene - Dialkyl alkylphosphonate - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Aryl halide - Phosphonic acid ester - Aryl chloride - Heteroaromatic compound - Imidazole - Azole - Organophosphonic acid derivative - Oxacycle - Azacycle - Organohalogen compound - Organooxygen compound - Organophosphorus compound - Primary amine - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organochloride - Aromatic heteropolycyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. |
| External Descriptors | Not available |
| Molekulargewicht | 423.800 g/mol |
|---|---|
| XLogP3 | 1.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 6 |
| Exact Mass | 423.086 Da |
| Monoisotopic Mass | 423.086 Da |
| Topological Polar Surface Area | 114.000 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 576.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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 |