4,4′-Azopyridine - ≥97% , CAS No.2632-99-7

CAS: 2632-99-7 Cat. No.: A486959 Formule: C₁₀H₈N₄ Poids moléculaire: 184.20 Numéro CE: 625-677-5

GRADE & PURITY ≥97%

Synonyms

4,4'-(1,2-diazenediyl)bis-pyridine | 4,4'-Azodipyridine | 4,4'-Azo-dipyridine | 4,4-AZO-DIPYRIDINE | 4,4'-(1E)-azobis-Pyridine | AKOS015955628 | 4,4'-Azobispyridine | SPHINGANINE [INCI] | 4-[(1E)-2-(pyridin-4-yl)diazen-1-yl]pyridine | AS-76296 | YSCK0253

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Wet ice

Vue d’ensemble

Description

4,4′-Azopyridine can be used:To prepare porous coordination polymers (PCPs) by reacting with Zn(NO3)2and 1,4-benzenedicarboxylic acid.As a reagent for the conversion of aliphatic alcohols into disulfides under Mitsunobu conditions.To prepare 4,4′-azopyridine-bridged binuclear zinc(II) complexes.Reactant for preparation of:Flexible porous coordination polymers constructed from 1,2-bis(4-pyridyl)hydrazine via solvothermal in situ reduction reactionMetal-organic frameworks based on transition-metal carboxylate clusters as secondary building unitsHeteroaromatic azo compounds under Mitsunobu conditionsMnII, CoII, and ZnII coordination polymersLow-dimensional and porous coordination compounds capable of supramolecular aromatic interactionsReagent in:Facile Mitsunobu esterification reactions

Specifications

Synonymes

4,4'-(1,2-diazenediyl)bis-pyridine | 4,4'-Azodipyridine | 4,4'-Azo-dipyridine | 4,4-AZO-DIPYRIDINE | 4,4'-(1E)-azobis-Pyridine | AKOS015955628 | 4,4'-Azobispyridine | SPHINGANINE [INCI] | 4-[(1E)-2-(pyridin-4-yl)diazen-1-yl]pyridine | AS-76296 | YSCK0253

Spécifications et pureté

≥97%

Conditions de stockage de stockage

Protected from light,Room temperature,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥97%

Noms et identifiants

• Pubchem Sid: 488188907
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188907
• Sourires canoniques: C1=CN=CC=C1N=NC2=CC=NC=C2
• IUPAC Name: dipyridin-4-yldiazene
• InChIKey: XUPMSLUFFIXCDA-UHFFFAOYSA-N
• INCHI: 1S/C10H8N4/c1-5-11-6-2-9(1)13-14-10-3-7-12-8-4-10/h1-8H
• Isomères SMILES: C1=CN=CC=C1N=NC2=CC=NC=C2
• WGK Allemagne: 3
• Numéro ONU: 2811
• Groupe d'emballage: III
• Poids moléculaire: 184.20
• Reaxy-Rn: 16342563
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=16342563&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Pyridines and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridines and derivatives
• Alternative Parents: Heteroaromatic compounds Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridine - Heteroaromatic compound - Azo compound - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
• 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

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive;Light and air sensitive
• Point de fusion (°C): 96-101 °C
• Poids moléculaire: 184.200 g/mol
• XLogP3: 1.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 184.075 Da
• Monoisotopic Mass: 184.075 Da
• Topological Polar Surface Area: 50.500 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 161.000
• 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

Références

1. Feitao Fan, Yiting Che, Vadim Efimov, Kuzmin Anton, Shitan Yan, Ting Bian.  (2025)  Hofmann-type MOFs derived small-sized Pt nanoparticles embedded in S, N codoped carbon matrix for enhanced oxygen reduction reaction.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2025.119545]

2. Maroof Ahmad Khan, Shaohui Huang, Xinfeng Du, Yongjie Yang, Yan Li, Yihui Yuan, Ning Wang.  (2026)  Bio-metal-organic framework with Nano-window traps for ultra-selective thorium separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2026.137179]