2,6-Dihydroxypyridine - ≥97% , CAS No.626-06-2

CAS: 626-06-2 Cat. No.: D304190 Fórmula: C₅H₅NO₂ Peso molecular: 111.10

GRADE & PURITY ≥97%

Synonyms

DIHYDROXYPYRIDINE, 2,6- | EINECS 210-927-4 | 2(1H)-Pyridinone, 6-hydroxy- | C03056 | SCHEMBL128525 | FT-0601051 | MFCD00129028 | 2-HYDROXY-6-PYRIDINONE | 6-hydroxy-1H-pyridin-2-one | Pyridine-2,6-diol | SY004410 | AS-31062 | 6-Hydroxy-2(1H)-pyridinone # |

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifications

Sinónimos

DIHYDROXYPYRIDINE, 2,6- | EINECS 210-927-4 | 2(1H)-Pyridinone, 6-hydroxy- | C03056 | SCHEMBL128525 | FT-0601051 | MFCD00129028 | 2-HYDROXY-6-PYRIDINONE | 6-hydroxy-1H-pyridin-2-one | Pyridine-2,6-diol | SY004410 | AS-31062 | 6-Hydroxy-2(1H)-pyridinone # |

Especificações e pureza

≥97%

Condições de armazenamento de armazenamento

Room temperature,Desiccated

Enviado em

Normal

Pureza

≥97%

Nomes e identificadores

• Pubchem Sid: 504754376
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754376
• Sorrisos canónicos: C1=CC(=O)NC(=C1)O
• IUPAC Name: 6-hydroxy-1H-pyridin-2-one
• InChIKey: WLFXSECCHULRRO-UHFFFAOYSA-N
• INCHI: 1S/C5H5NO2/c7-4-2-1-3-5(8)6-4/h1-3H,(H2,6,7,8)
• SMILES isoméricas: C1=CC(=O)NC(=C1)O
• Peso molecular: 111.10
• Reaxy-Rn: 1524318
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1524318&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Pyridines and derivatives
      • Subclass Hydropyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Pyridines and derivatives
• Subclass: Hydropyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinones
• Alternative Parents: Hydroxypyridines Dihydropyridines Heteroaromatic compounds Lactams Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Hydroxypyridine - Pyridinone - Dihydropyridine - Heteroaromatic compound - Lactam - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as pyridinones. These are compounds containing a pyridine ring, which bears a ketone.
• External Descriptors: a small molecule

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

Mecanismos de ação

Propriedades químicas e físicas

• Peso molecular: 111.100 g/mol
• XLogP3: 0.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 111.032 Da
• Monoisotopic Mass: 111.032 Da
• Topological Polar Surface Area: 49.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 169.000
• 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

Referências

1. Yucheng Yang, Siwei Yang, Guqiao Ding, Zhi Liu.  (2020)  Self-feedback autocatalysis in free radical triggered photosynthesis of N-doped graphene quantum dots.  SYNTHETIC METALS,      [PMID:] [10.1016/j.synthmet.2020.116643]

2. Jiao Yuchen, Zhou Ming, Pu Bo, Yang Xiaoling, Li Chenyiting, Xia Liangliang, Deng Guilin, Wei Yunyao, Zhong Jing, Wu Zheng, Chen Shi, Wang Jian, Zhou Yujun.  (2026)  Preparation of room-temperature self-healing recyclable polyurethane elastomers based on a multiple hydrogen/nitrogen coordination boro-oxygen bonds system.  JOURNAL OF POLYMER RESEARCH,  33  (3): (114).  [PMID:] [10.1007/s10965-025-04746-w]