2-Amino-5-bromopyridine - ≥98% , CAS No.1072-97-5

CAS: 1072-97-5 Cat. No.: A101197 Molecular Weight: 173.01 Beilstein Registry Number: 108737 EC Number: 214-019-9

GRADE & PURITY ≥98%

Synonyms

AC-907/34116004 | MFCD02234511 | STK024650 | MFCD00006323 | STR04388 | 2-Amino-5-bromopyridine, 97% | 5-Bromo-2-aminopyridine | 5-bromo-2-amino-pyridine | FT-0611152 | DTXSID5022144 | 5-Bromo-2-pyridylamine | 2-Amino-5-bromopyridine | 2-amino-5-bromo-pyri

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Overview

2-Amino-5-bromopyridine is a brominated aromatic amine reagent and is used for labeling of model reducing-end oligosaccharides via reductive amination.

Specifications

Synonyms

AC-907/34116004 | MFCD02234511 | STK024650 | MFCD00006323 | STR04388 | 2-Amino-5-bromopyridine, 97% | 5-Bromo-2-aminopyridine | 5-bromo-2-amino-pyridine | FT-0611152 | DTXSID5022144 | 5-Bromo-2-pyridylamine | 2-Amino-5-bromopyridine | 2-amino-5-bromo-pyri

Specifications & Purity

≥98%

Storage

Protected from light, Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504754549
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754549
• Canonical Smiles: C1=CC(=NC=C1Br)N
• IUPAC Name: 5-bromopyridin-2-amine
• InChIKey: WGOLHUGPTDEKCF-UHFFFAOYSA-N
• INCHI: 1S/C5H5BrN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
• Isomeric SMILES: C1=CC(=NC=C1Br)N
• WGK Germany: 2
• Alternate CAS: 1072-97-5
• NSC Number: 26282
• UN Number: 2811
• MeSH Entry Terms: 2-amino-5-bromopyridine
• Molecular Weight: 173.01
• Beilstein: 108737
• Reaxy-Rn: 108737
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=108737&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyridines and derivatives
• Subclass: Aminopyridines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Aminopyridines and derivatives
• Alternative Parents: Imidolactams Aryl bromides Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aminopyridine - Imidolactam - Aryl halide - Aryl bromide - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organobromide - Organohalogen compound - Amine - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring.
• 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 methanol, chloroform, ethyl acetate. Slightly soluble in water.
• Sensitivity: Light sensitive
• Melt Point(°C): 133-138°C
• Molecular Weight: 173.010 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 171.964 Da
• Monoisotopic Mass: 171.964 Da
• Topological Polar Surface Area: 38.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 76.800
• 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. Xianwu Jiang, Zhuodong Sun, Yu Wang.  (2022)  Solvent-Free and Efficient One-Pot Strategy for Synthesis of the Triazine-Heterocycle Azacyanines.  Materials,  15  (7): (2619).  [PMID:35407951] [10.3390/ma15072619]