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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Bropirimine - ≥98%(HPLC) , CAS No.56741-95-8
Synonyms
4(3H)-Pyrimidinone, 2-amino-5-bromo-6-phenyl- | Bropirimine | BROPIRIMINE [JAN] | SCHEMBL4058 | AB00081669-01 | CHEBI:31307 | J-501991 | A831159 | UNII-J57CTF25XJ | Z1272069497 | BROPIRIMINE [INN] | Bropiriminum | EN300-235927 | FT-0602773 | 1rsi | 2-Amin
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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.
Specifications Sinónimos
4(3H)-Pyrimidinone, 2-amino-5-bromo-6-phenyl- | Bropirimine | BROPIRIMINE [JAN] | SCHEMBL4058 | AB00081669-01 | CHEBI:31307 | J-501991 | A831159 | UNII-J57CTF25XJ | Z1272069497 | BROPIRIMINE [INN] | Bropiriminum | EN300-235927 | FT-0602773 | 1rsi | 2-Amin
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Immunomodulatory and antitumor compound. Induces interferon (IFN)-α/βproduction; augments natural killer (NK) cell activity. Orally active.
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 504773284 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504773284 Sonrisas canónicas C1=CC=C(C=C1)C2=C(C(=O)NC(=N2)N)Br IUPAC Name 2-amino-5-bromo-4-phenyl-1H-pyrimidin-6-one InChIKey CIUUIPMOFZIWIZ-UHFFFAOYSA-N INCHI 1S/C10H8BrN3O/c11-7-8(6-4-2-1-3-5-6)13-10(12)14-9(7)15/h1-5H,(H3,12,13,14,15) Isómeros SMILES C1=CC=C(C=C1)C2=C(C(=O)NC(=N2)N)Br WGK Alemania 3 RTECS UW7351300 Peso molecular 266.09 Reaxy-Rn 651807 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=651807&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 Clase Diazines Subclass Pyrimidines and pyrimidine derivatives Intermediate Tree Nodes Not available Direct Parent Phenylpyrimidines Alternative Parents Pyrimidones Halopyrimidines Aminopyrimidines and derivatives Hydropyrimidines Benzene and substituted derivatives Aryl bromides Vinylogous amides Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organobromides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents 4-phenylpyrimidine - 5-phenylpyrimidine - Aminopyrimidine - Halopyrimidine - Pyrimidone - Benzenoid - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Azacycle - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Amine - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as phenylpyrimidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrimidine ring through a CC or CN bond. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. External Descriptors pyrimidines 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:DMSO, Max Conc. mg/mL: 26.61, Max Conc. mM: 100 Peso molecular 266.090 g/mol XLogP3 1.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 1 Exact Mass 264.985 Da Monoisotopic Mass 264.985 Da Topological Polar Surface Area 67.500 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 343.000 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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