2,6-Dibromopyridine - ≥98% , CAS No.626-05-1

CAS: 626-05-1 Cat. No.: D101563 Molecular Weight: 236.89 Beilstein Registry Number: 108922 EC Number: 210-926-9

GRADE & PURITY ≥98%

Synonyms

2.6-dibromopyridine | A937236 | 2,6-dibrompyridine | 2,6-Dibromopyridine, 98% | EINECS 210-926-9 | GEO-00971 | STR02550 | W-203332 | 2,6-Dibromopyridine, | HY-59162 | 2, 6-Dibromopyridine | D1555 | MFCD00006223 | Q209274 | AM81197 | PYRIDINE, 2,6-DIBROMO-

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Synonyms

2.6-dibromopyridine | A937236 | 2, 6-dibrompyridine | 2, 6-Dibromopyridine, 98% | EINECS 210-926-9 | GEO-00971 | STR02550 | W-203332 | 2, 6-Dibromopyridine, | HY-59162 | 2, 6-Dibromopyridine | D1555 | MFCD00006223 | Q209274 | AM81197 | PYRIDINE, 2, 6-DIBROMO-

Specifications & Purity

≥98%

Storage

Protected from light, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488181600
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181600
• Canonical Smiles: C1=CC(=NC(=C1)Br)Br
• IUPAC Name: 2,6-dibromopyridine
• InChIKey: FEYDZHNIIMENOB-UHFFFAOYSA-N
• INCHI: 1S/C5H3Br2N/c6-4-2-1-3-5(7)8-4/h1-3H
• Isomeric SMILES: C1=CC(=NC(=C1)Br)Br
• WGK Germany: 3
• RTECS: US7883000
• Molecular Weight: 236.89
• Beilstein: 108922
• Reaxy-Rn: 108922
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=108922&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyridines and derivatives
      • Subclass Halopyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyridines and derivatives
• Subclass: Halopyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Polyhalopyridines
• Alternative Parents: 2-halopyridines Aryl bromides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Polyhalopyridine - 2-halopyridine - Aryl halide - Aryl bromide - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as polyhalopyridines. These are organic compounds containing a pyridine ring substituted at two or more positions by a halogen atom.
• 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

Chemical and Physical Properties

• Solubility: Soluble in hot methanol. Insoluble in water.
• Sensitivity: Light sensitive.
• Flash Point(°F): >212 °F
• Flash Point(°C): >100 °C
• Boil Point(°C): 249°C
• Melt Point(°C): 118-119 ºC
• Molecular Weight: 236.890 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 236.861 Da
• Monoisotopic Mass: 234.863 Da
• Topological Polar Surface Area: 12.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 68.800
• 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

References

1. Yana Zhang, Jiaoyang Chen, Guangpu Zhang, Jianqiang Xv, Jianhua Xv, Yubing Hu, Hu Guo, Fan guo, JiaJun Fu, Wei Jiang.  (2021)  Mechanically robust, highly adhesive and autonomously low-temperature self-healing elastomer fabricated based on dynamic metal − ligand interactions tailored for functional energetic composites.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.130665]