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Atomfair 3,5-Dichloro-3-pyridylamine C5H4Cl2N2

Description 3,5-Dichloro-3-pyridylamine (CAS No. 4214-74-8) is a high-purity heterocyclic organic compound with the molecular formula C5H4Cl2N2. This fine chemical, also known by its IUPAC name 3,5-dichloropyridin-2-amine , is a valuable intermediate in pharmaceutical and agrochemical synthesis. The compound features a pyridine ring substituted with two chlorine atoms at the 3 and 5 positions and an amine group at the 2 position, offering versatile reactivity for nucleophilic substitution and cross-coupling reactions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder under inert packaging to maintain stability. Suitable for research and…

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Description

Description

3,5-Dichloro-3-pyridylamine (CAS No. 4214-74-8) is a high-purity heterocyclic organic compound with the molecular formula C5H4Cl2N2. This fine chemical, also known by its IUPAC name 3,5-dichloropyridin-2-amine, is a valuable intermediate in pharmaceutical and agrochemical synthesis. The compound features a pyridine ring substituted with two chlorine atoms at the 3 and 5 positions and an amine group at the 2 position, offering versatile reactivity for nucleophilic substitution and cross-coupling reactions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder under inert packaging to maintain stability. Suitable for research and development in medicinal chemistry, this compound is packaged in amber glass vials or bulk quantities with comprehensive analytical data (MSDS, NMR, HPLC) available upon request.

  • CAS No: 4214-74-8
  • Molecular Formula: C5H4Cl2N2
  • Molecular Weight: 163.00
  • Exact Mass: 161.9751535
  • Monoisotopic Mass: 161.9751535
  • IUPAC Name: 3,5-dichloropyridin-2-amine
  • SMILES: C1=C(C=NC(=C1Cl)N)Cl
  • Synonyms: 2-Amino-3,5-dichloropyridine, 4214-74-8, 3,5-Dichloro-3-pyridylamine, EINECS 224-143-5, DTXSID80194976

Application

3,5-Dichloro-3-pyridylamine serves as a key building block in the synthesis of advanced pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. It is widely utilized in agrochemical research for creating novel pesticides and herbicides due to its bioactive pyridine core. The compound’s reactive sites enable facile functionalization for structure-activity relationship (SAR) studies in drug discovery programs.

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