clorhidrato de 2,5-diamino-4,6-dihidroxipirimidina - ≥98%(HPLC) , CAS No.56830-58-1

CAS: 56830-58-1 Cat. No.: D133500 Peso molecular: 178.58 Número EC: 611-428-8

GRADE & PURITY ≥98%(HPLC)

Synonyms

4(1H)-Pyrimidinone, 2,5-diamino-6-hydroxy-, monohydrochloride | AMY4031 | 2,5-Diamino-4,6-dihydroxy-pyrimidine | SCHEMBL655381 | AS-68025 | 2,5-Diamino-6-hydroxy-4(1H)-pyrimidinone Hydrochloride | BCP13016 | W-203142 | 2,5-diamino-4-hydroxy-1H-pyrimidin-6

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

4(1H)-Pyrimidinone, 2, 5-diamino-6-hydroxy-, monohydrochloride | AMY4031 | 2, 5-Diamino-4, 6-dihydroxy-pyrimidine | SCHEMBL655381 | AS-68025 | 2, 5-Diamino-6-hydroxy-4(1H)-pyrimidinone Hydrochloride | BCP13016 | W-203142 | 2, 5-diamino-4-hydroxy-1H-pyrimidin-6

Especificaciones y pureza

≥98%(HPLC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(HPLC)

Nombres e identificadores

• Pubchem Sid: 488192462
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192462
• Sonrisas canónicas: C1(=C(N=C(NC1=O)N)O)N.Cl
• IUPAC Name: 2,5-diamino-4-hydroxy-1H-pyrimidin-6-one;hydrochloride
• InChIKey: IIVYOQGIZSPVFZ-UHFFFAOYSA-N
• INCHI: 1S/C4H6N4O2.ClH/c5-1-2(9)7-4(6)8-3(1)10;/h5H2,(H4,6,7,8,9,10);1H
• Isómeros SMILES: C1(=C(N=C(NC1=O)N)O)N.Cl
• Peso molecular: 178.58
• Reaxy-Rn: 3632170
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3632170&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Diazines
      • Subclass Pyrimidines and pyrimidine derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Diazines
• Subclass: Pyrimidines and pyrimidine derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroxypyrimidines
• Alternative Parents: Pyrimidones Aminopyrimidines and derivatives Hydropyrimidines Vinylogous acids Heteroaromatic compounds Lactams Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aminopyrimidine - Pyrimidone - Hydroxypyrimidine - Hydropyrimidine - Vinylogous acid - Heteroaromatic compound - Lactam - Azacycle - Hydrochloride - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydroxypyrimidines. These are organic compounds containing a hydroxyl group attached to a pyrimidine ring. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
• 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.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Peso molecular: 178.580 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 178.026 Da
• Monoisotopic Mass: 178.026 Da
• Topological Polar Surface Area: 114.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 242.000
• 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: 2

XLogP3

Referencias

1. Hongwei Zhu, Lianghe Sun, Ming Lu, Yuangang Xu.  (2025)  Synthesis and characterization of a series of cyclo-N5− salts with layered stacking patterns.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2025.143111]