2-Amino-5-nitropyridine - ≥98% , CAS No.4214-76-0

CAS: 4214-76-0 Cat. No.: A124302 Peso molecular: 139.11 Beilstein Registry Number: 120353 Número EC: 224-145-6

GRADE & PURITY ≥98%

Synonyms

2-Amino-5-nitropyridine, 97% | EN300-21336 | A0794 | GEO-00192 | SCHEMBL116229 | STK801376 | 2-Amino-5-nitropyridine, technical, >=95.0% (NT) | EINECS 224-145-6 | DTXSID6063357 | 5-Nitropyridine-2-amine | STR05721 | 2-Pyridinamine, 5-nitro- | 5-Nitro-2-py

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Sinónimos

2-Amino-5-nitropyridine, 97% | EN300-21336 | A0794 | GEO-00192 | SCHEMBL116229 | STK801376 | 2-Amino-5-nitropyridine, technical, >=95.0% (NT) | EINECS 224-145-6 | DTXSID6063357 | 5-Nitropyridine-2-amine | STR05721 | 2-Pyridinamine, 5-nitro- | 5-Nitro-2-py

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488185479
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185479
• Sonrisas canónicas: C1=CC(=NC=C1[N+](=O)[O-])N
• IUPAC Name: 5-nitropyridin-2-amine
• InChIKey: UGSBCCAHDVCHGI-UHFFFAOYSA-N
• INCHI: 1S/C5H5N3O2/c6-5-2-1-4(3-7-5)8(9)10/h1-3H,(H2,6,7)
• Isómeros SMILES: C1=CC(=NC=C1[N+](=O)[O-])N
• WGK Alemania: 3
• Peso molecular: 139.11
• Beilstein: 120353
• Reaxy-Rn: 120353
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=120353&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic 1,3-dipolar compounds
    • Clase Allyl-type 1,3-dipolar organic compounds
      • Subclass Organic nitro compounds
        • Level5 C-nitro compounds
          • Level6 Nitroaromatic compounds

• Kingdom: Organic compounds
• Superclass: Organic 1,3-dipolar compounds
• Clase: Allyl-type 1,3-dipolar organic compounds
• Subclass: Organic nitro compounds
• Intermediate Tree Nodes: C-nitro compounds
• Direct Parent: Nitroaromatic compounds
• Alternative Parents: Aminopyridines and derivatives Imidolactams Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Nitroaromatic compound - Aminopyridine - Pyridine - Imidolactam - Heteroaromatic compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Organopnictogen compound - Primary amine - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
• 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

• Solubilidad: Soluble in Methanol,Chloroform
• Sensibilidad: Light Sensitive
• Punto de inflamación (°F): 224℃(435°F)
• Punto de inflamación (°C): 224℃(435°F)
• Punto de fusión (°C): 185-190°C
• Peso molecular: 139.110 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 139.038 Da
• Monoisotopic Mass: 139.038 Da
• Topological Polar Surface Area: 84.700 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 133.000
• 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. Fu Fengping, He Qian, Zhao Shizheng, Zhu Ting, Liao Fang.  (2021)  Synthesis of photoluminescent m-phenylenediamine-Rhodamine B copolymer dots: selective ultrahigh photocatalytic performance for catalytic reduction of nitro-compound.  RESEARCH ON CHEMICAL INTERMEDIATES,  47  (10): (4173-4192).  [PMID:] [10.1007/s11164-021-04512-9]