Cas no 1227595-65-4 (4-chloro-3-(trifluoromethyl)pyridin-2-amine)

4-Chloro-3-(trifluoromethyl)pyridin-2-amine is a fluorinated pyridine derivative with significant utility in pharmaceutical and agrochemical research. Its structure, featuring both chloro and trifluoromethyl substituents, enhances reactivity and stability, making it a valuable intermediate in the synthesis of bioactive compounds. The trifluoromethyl group contributes to improved metabolic stability and lipophilicity, while the chloro substituent allows for further functionalization. This compound is particularly useful in the development of herbicides, fungicides, and pharmaceutical candidates targeting diverse biological pathways. Its high purity and consistent performance ensure reliable results in synthetic applications. Researchers favor this intermediate for its versatility in constructing complex heterocyclic frameworks.
4-chloro-3-(trifluoromethyl)pyridin-2-amine structure
1227595-65-4 structure
Product Name:4-chloro-3-(trifluoromethyl)pyridin-2-amine
CAS No:1227595-65-4
MF:C6H4ClF3N2
MW:196.557570457458
CID:2618219
PubChem ID:68849469
Update Time:2025-11-01

4-chloro-3-(trifluoromethyl)pyridin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 4-chloro-3-(trifluoromethyl)pyridin-2-amine
    • AB70883
    • 2-AMINO-4-CHLORO-3-(TRIFLUOROMETHYL)PYRIDINE
    • SCHEMBL3945531
    • 1227595-65-4
    • Inchi: 1S/C6H4ClF3N2/c7-3-1-2-12-5(11)4(3)6(8,9)10/h1-2H,(H2,11,12)
    • InChI Key: QDTVQKKWZAYRBU-UHFFFAOYSA-N
    • SMILES: ClC1C=CN=C(C=1C(F)(F)F)N

Computed Properties

  • Exact Mass: 196.0015103Da
  • Monoisotopic Mass: 196.0015103Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 161
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2
  • Topological Polar Surface Area: 38.9?2

4-chloro-3-(trifluoromethyl)pyridin-2-amine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
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Additional information on 4-chloro-3-(trifluoromethyl)pyridin-2-amine

Comprehensive Overview of 4-chloro-3-(trifluoromethyl)pyridin-2-amine (CAS No. 1227595-65-4)

4-chloro-3-(trifluoromethyl)pyridin-2-amine (CAS No. 1227595-65-4) is a specialized pyridine derivative widely recognized for its unique chemical properties and applications in pharmaceutical and agrochemical research. This compound, characterized by its chloro and trifluoromethyl functional groups, has garnered significant attention due to its potential as a building block in drug discovery and material science. Researchers and industry professionals frequently search for terms like "synthesis of 4-chloro-3-(trifluoromethyl)pyridin-2-amine", "applications of trifluoromethyl pyridines", and "CAS 1227595-65-4 suppliers", reflecting its growing relevance in modern chemistry.

The structural features of 4-chloro-3-(trifluoromethyl)pyridin-2-amine make it a valuable intermediate in the development of bioactive molecules. The presence of the trifluoromethyl group enhances the compound's metabolic stability and lipophilicity, traits highly sought after in medicinal chemistry. Recent studies highlight its role in designing kinase inhibitors and antimicrobial agents, aligning with the current focus on targeted therapies and antibiotic resistance. Searches for "pyridine derivatives in drug design" and "trifluoromethyl compounds in pharmaceuticals" underscore the compound's intersection with cutting-edge research trends.

From a synthetic perspective, CAS No. 1227595-65-4 is often prepared via nucleophilic substitution or palladium-catalyzed coupling reactions. Optimizing its yield and purity remains a topic of interest, as evidenced by queries like "efficient synthesis of 4-chloro-3-(trifluoromethyl)pyridin-2-amine". The compound's stability under various conditions also makes it a candidate for high-throughput screening libraries, a hotspot in AI-driven drug discovery platforms. This aligns with the surge in searches for "computational chemistry tools for heterocycles" and "fragment-based drug design".

In agrochemical applications, 4-chloro-3-(trifluoromethyl)pyridin-2-amine serves as a precursor for herbicides and pesticides, addressing the global demand for sustainable crop protection. Its halogenated pyridine core contributes to the development of compounds with enhanced environmental compatibility, resonating with searches for "green chemistry in agrochemicals" and "low-residue pesticides". Regulatory compliance and safety profiles of such derivatives are frequently discussed, reflecting industry priorities.

Analytical characterization of CAS 1227595-65-4 typically involves techniques like HPLC, NMR, and mass spectrometry, with researchers often inquiring about "spectral data for 4-chloro-3-(trifluoromethyl)pyridin-2-amine". The compound's compatibility with flow chemistry and continuous manufacturing processes further positions it as a fit for modern industrial workflows, a trend mirrored in searches for "scalable synthesis of fluorinated pyridines".

As the scientific community prioritizes structure-activity relationship (SAR) studies, 4-chloro-3-(trifluoromethyl)pyridin-2-amine continues to be a subject of patents and publications. Its versatility in generating analog libraries aligns with the rise of precision medicine and personalized therapeutics, topics dominating academic and industrial discourse. This compound exemplifies how heterocyclic chemistry bridges fundamental research and real-world solutions, answering pressing questions in health and agriculture.

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