6-Amino-4-hydroxy-2-mercaptopyrimidine - ≥98% , CAS No.1004-40-6

CAS: 1004-40-6 Cat. No.: A189279 Peso molecular: 143.17

GRADE & PURITY ≥98%

Synonyms

6-Amino-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone # | 6-amino-2-sulfanylpyrimidin-4(3H)-one | 6-amino-2-thioxo-1H-pyrimidin-4-one | 6-Amino-4-hydroxy-2-mercaptopyrimidine | 6-amino-4-hydroxy-2-mercapto-pyrimidine | AC-26630 | EN300-33998 | 6-amino-2-sulfany

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

6-Amino-2-thioxo-2, 3-dihydro-4(1H)-pyrimidinone # | 6-amino-2-sulfanylpyrimidin-4(3H)-one | 6-amino-2-thioxo-1H-pyrimidin-4-one | 6-Amino-4-hydroxy-2-mercaptopyrimidine | 6-amino-4-hydroxy-2-mercapto-pyrimidine | AC-26630 | EN300-33998 | 6-amino-2-sulfany

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488191737
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488191737
• Sonrisas canónicas: C1=C(NC(=S)NC1=O)N
• IUPAC Name: 6-amino-2-sulfanylidene-1H-pyrimidin-4-one
• InChIKey: YFYYRKDBDBILSD-UHFFFAOYSA-N
• INCHI: 1S/C4H5N3OS/c5-2-1-3(8)7-4(9)6-2/h1H,(H4,5,6,7,8,9)
• Isómeros SMILES: C1=C(NC(=S)NC1=O)N
• Peso molecular: 143.17
• Reaxy-Rn: 120629
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=120629&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: Pyrimidones
• Alternative Parents: Pyrimidinethiones Aminopyrimidines and derivatives 2-Thiopyrimidines Hydropyrimidines Vinylogous amides Heteroaromatic compounds Thioureas Lactams Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aminopyrimidine - 2-thiopyrimidine - Thiopyrimidine - Pyrimidinethione - Pyrimidone - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Lactam - Thiourea - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyrimidones. These are compounds that contain a pyrimidine ring, which bears a ketone. 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

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 143.170 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 143.015 Da
• Monoisotopic Mass: 143.015 Da
• Topological Polar Surface Area: 99.200 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 198.000
• 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

Referencias

1. Bingyan Han, Yajun Chen, Qingdong Liu, Yuncong Gao, Jiao Wang, Haiyan Liu, Gaohong He.  (2024)  H2O rapidly constructs hydrogen bond networks to reinforce AIE of copper clusters: Fluorescence discoloration and enhanced behavior for alcohol content detection and latent fingerprints recognition.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.128211]