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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Besifovir - ≥96% , CAS No.441785-25-7
Disponível para encomenda
Synonyms
s6729 | D96121 | [1-[(2-aminopurin-9-yl)methyl]cyclopropyl]oxymethylphosphonic acid | SCHEMBL2908200 | Besifovir | BESIFOVIR [WHO-DD] | HY-19447 | FT-0653031 | Q27260336 | Besifovir [INN] | KDNSSKPZBDNJDF-UHFFFAOYSA-N | [1-[(2-aminopurin-9-yl)methyl]cyclo
Shipped In
Ice chest + Ice pads
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Why this grade ≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Visão geral Information
Besifovir Besifovir is novel and potent acyclic nucleotide phosphonate used to treat hepatitis B virus (HBV) infection.
Specifications Sinónimos
s6729 | D96121 | [1-[(2-aminopurin-9-yl)methyl]cyclopropyl]oxymethylphosphonic acid | SCHEMBL2908200 | Besifovir | BESIFOVIR [WHO-DD] | HY-19447 | FT-0653031 | Q27260336 | Besifovir [INN] | KDNSSKPZBDNJDF-UHFFFAOYSA-N | [1-[(2-aminopurin-9-yl)methyl]cyclo
Especificações e pureza
≥96%
Mecanismos bioquímicos e fisiológicos
Besifovir is novel and potent acyclic nucleotide phosphonate used to treat hepatitis B virus (HBV) infection.
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504763285
Sorrisos canónicos
C1CC1(CN2C=NC3=CN=C(N=C32)N)OCP(=O)(O)O
IUPAC Name
[1-[(2-aminopurin-9-yl)methyl]cyclopropyl]oxymethylphosphonic acid
InChIKey
KDNSSKPZBDNJDF-UHFFFAOYSA-N
INCHI
1S/C10H14N5O4P/c11-9-12-3-7-8(14-9)15(5-13-7)4-10(1-2-10)19-6-20(16,17)18/h3,5H,1-2,4,6H2,(H2,11,12,14)(H2,16,17,18)
SMILES isoméricas
C1CC1(CN2C=NC3=CN=C(N=C32)N)OCP(=O)(O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9717556&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Classe Imidazopyrimidines Subclass Purines and purine derivatives Intermediate Tree Nodes Not available Direct Parent Purines and purine derivatives Alternative Parents Aminopyrimidines and derivatives N-substituted imidazoles Organic phosphonic acids Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Purine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - Heteroaromatic compound - Azacycle - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Amine - Organic oxygen compound - Primary amine - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as purines and purine derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Solubilidade Solubility (25°C) In vitro DMSO: 60 mg/mL (200.52 mM); Water: 60 mg/mL (200.52 mM); Ethanol: 2 mg/mL (6.68 mM); Peso molecular 299.220 g/mol XLogP3 -1.800 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 5 Exact Mass 299.078 Da Monoisotopic Mass 299.078 Da Topological Polar Surface Area 136.000 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 414.000 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
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