GRADE & PURITY ≥98%

Synonyms

2-amino-5-chloro pyridine | InChI=1/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8 | RP-26695 | SY001089 | 5-chloro-pyridin-2-ylamine | 5-chloropyridin-2-ylamine | 2-AMino-5-chloropyridine--d3 | STK398098 | 2-amino-5-chloropyridin | AC-2429 | J8TAP6NFD4 | 2-am

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

2-amino-5-chloro pyridine | InChI=1/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H, (H2, 7, 8 | RP-26695 | SY001089 | 5-chloro-pyridin-2-ylamine | 5-chloropyridin-2-ylamine | 2-AMino-5-chloropyridine--d3 | STK398098 | 2-amino-5-chloropyridin | AC-2429 | J8TAP6NFD4 | 2-am

Specifications & Purity

≥98%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488183752
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183752
• Canonical Smiles: C1=CC(=NC=C1Cl)N
• IUPAC Name: 5-chloropyridin-2-amine
• InChIKey: MAXBVGJEFDMHNV-UHFFFAOYSA-N
• INCHI: 1S/C5H5ClN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
• Isomeric SMILES: C1=CC(=NC=C1Cl)N
• WGK Germany: 3
• Molecular Weight: 128.56
• Beilstein: 108735
• Reaxy-Rn: 108735
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=108735&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 chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aminopyridine - Imidolactam - Aryl halide - Aryl chloride - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organochloride - 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

• Sensitivity: Light & Air Sensitive.
• Flash Point(°F): 320 °F
• Flash Point(°C): 160 °C
• Boil Point(°C): 127-128°C
• Melt Point(°C): 134-138°C
• Molecular Weight: 128.560 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 128.014 Da
• Monoisotopic Mass: 128.014 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. Liu Weixiang, Qin Yukun, Liu Song, Xing Ronge, Yu Huahua, Chen Xiaolin, Li Kecheng, Li Pengcheng.  (2018)  Synthesis of C-coordinated O-carboxymethyl chitosan metal complexes and evaluation of their antifungal activity.  Scientific Reports,  8  (1): (1-10).  [PMID:29556071] [10.1038/s41598-018-23283-9]