Cas no 1163681-50-2 (3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine)

3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine is a halogenated pyridine derivative featuring a trifluoromethyl group and a phenylamino substituent. This compound is of interest in agrochemical and pharmaceutical research due to its structural motifs, which are known to enhance biological activity and metabolic stability. The presence of the chloro and trifluoromethyl groups contributes to its potential as an intermediate in the synthesis of active ingredients for crop protection or medicinal chemistry applications. Its well-defined molecular structure allows for precise modifications, making it a valuable building block in the development of novel compounds with tailored properties.
3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine structure
1163681-50-2 structure
Product Name:3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine
CAS No:1163681-50-2
MF:C12H8ClF3N2
MW:272.653532028198
CID:4682724
Update Time:2025-05-19

3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine Chemical and Physical Properties

Names and Identifiers

    • 3-chloro-N-phenyl-5-(trifluoromethyl)pyridin-2-amine
    • 3-CHLORO-N-PHENYL-5-(TRIFLUOROMETHYL)-2-PYRIDINAMINE
    • 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine
    • Inchi: 1S/C12H8ClF3N2/c13-10-6-8(12(14,15)16)7-17-11(10)18-9-4-2-1-3-5-9/h1-7H,(H,17,18)
    • InChI Key: PRKIKMBVUOYEDJ-UHFFFAOYSA-N
    • SMILES: ClC1=CC(C(F)(F)F)=CN=C1NC1C=CC=CC=1

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 267
  • Topological Polar Surface Area: 24.9

3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
C045465-125mg
3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine
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$ 230.00 2022-06-01
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Additional information on 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine

Comprehensive Overview of 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine (CAS No. 1163681-50-2)

3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine (CAS No. 1163681-50-2) is a specialized chemical compound that has garnered significant attention in the fields of agrochemical and pharmaceutical research. This compound, characterized by its unique molecular structure featuring a chloro and trifluoromethyl substituents, plays a pivotal role in the development of advanced intermediates for various applications. Researchers and industry professionals are increasingly interested in its synthesis, properties, and potential uses, making it a subject of frequent queries in scientific databases and AI-driven search platforms.

The growing demand for trifluoromethylpyridine derivatives in modern chemistry has positioned 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine as a key compound. Its structural features, including the phenylamine moiety, contribute to its reactivity and versatility. Recent studies highlight its relevance in the design of novel crop protection agents and pharmaceutical intermediates, aligning with the global focus on sustainable agriculture and precision medicine. Searches for "trifluoromethylpyridine applications" and "chloropyridinamine synthesis" have surged, reflecting its importance in contemporary research.

From a synthetic perspective, CAS No. 1163681-50-2 is often explored for its potential in cross-coupling reactions and catalytic transformations. The presence of both chloro and trifluoromethyl groups offers distinct reactivity patterns, enabling chemists to tailor its derivatives for specific functions. This adaptability has led to its inclusion in high-throughput screening programs, particularly in the search for bioactive molecules with enhanced efficacy and selectivity.

In the context of environmental and regulatory trends, 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine is scrutinized for its eco-friendly synthesis routes and green chemistry compatibility. As industries shift toward sustainable practices, queries like "green synthesis of pyridinamines" and "low-impact agrochemical intermediates" have become prevalent. Researchers are actively investigating solvent-free or catalytic methods to produce this compound, minimizing waste and energy consumption.

The compound’s physicochemical properties, such as solubility, stability, and bioavailability, are also critical to its applications. Analytical techniques like HPLC, NMR, and mass spectrometry are routinely employed to characterize CAS No. 1163681-50-2 and its derivatives. These methods ensure compliance with stringent quality standards, particularly in pharmaceutical-grade intermediates and agrochemical formulations.

Looking ahead, 3-Chloro-N-phenyl-5-(trifluoromethyl)-2-pyridinamine is poised to remain a focal point in innovation-driven sectors. Its integration into AI-assisted drug discovery platforms and computational chemistry models underscores its relevance in the digital age. By addressing common search queries such as "pyridinamine derivatives in drug design" and "trifluoromethyl group effects," this overview bridges the gap between academic research and industrial demand, offering actionable insights for stakeholders.

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