Cas no 7059-61-2 (6-Chloropyridine-2-carboxylic acid amide)

6-Chloropyridine-2-carboxylic acid amide structure
7059-61-2 structure
Product Name:6-Chloropyridine-2-carboxylic acid amide
CAS No:7059-61-2
MF:C6H5ClN2O
MW:156.56970000267
CID:1076441
PubChem ID:302933
Update Time:2025-07-19

6-Chloropyridine-2-carboxylic acid amide Chemical and Physical Properties

Names and Identifiers

    • 6-Chloropyridine-2-carboxylic acid amide
    • 1,3-bis-[3-(3-ethyl-3H-benzothiazol-2-ylidene)-propenyl]-5,5-dimethyl-cyclohex-1-> 3-enylium,
    • 1,3-Bis-[3-(4-fluor-phenyl)-3-oxo-prop-1-enyl]-benzol
    • 3-ethyl-2-(3-{3-[3-(3-ethyl-3H-benzothiazol-2-ylidene)-propenyl]-5,5-dimethyl-cyclohex-2-enylidene}-propenyl)-benzothiazolium, iodide
    • 3-ETHYL-2-[(E)-3-(3-((E)-3-[3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE]-1-ALLYL)-5,5-DIMETHYL-2-CYCLOHEXEN-1-YLIDENE)-1-ALLYL]-1,3-BENZOTHIAZOL-3-IUM IODIDE
    • A26072
    • AKOS003624847
    • Z969100498
    • 6-Chloropicolinamide
    • EN300-130272
    • NSC190685
    • 6-chloropyridine-2-carboxamide
    • FT-0722957
    • 6-Chloropyridine-2-carboxylic acid amide, AldrichCPR
    • 7059-61-2
    • 70593-61-2
    • J-518639
    • DTXSID80990814
    • NSC-190685
    • SB52403
    • FT-0681651
    • GIVBFKYXAXLZBT-UHFFFAOYSA-N
    • MFCD00708892
    • Oprea1_039984
    • CS-0119862
    • SDCCGMLS-0064546.P001
    • TS-02079
    • SCHEMBL2828415
    • 2-Pyridinecarboxamide, 6-chloro-
    • DB-081941
    • ALBB-022380
    • STK801780
    • BBL028889
    • Inchi: 1S/C6H5ClN2O/c7-5-3-1-2-4(9-5)6(8)10/h1-3H,(H2,8,10)
    • InChI Key: GIVBFKYXAXLZBT-UHFFFAOYSA-N
    • SMILES: ClC1=CC=CC(C(N)=O)=N1

Computed Properties

  • Exact Mass: 156.0090405g/mol
  • Monoisotopic Mass: 156.0090405g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 140
  • 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: 1
  • Topological Polar Surface Area: 56?2

6-Chloropyridine-2-carboxylic acid amide Security Information

  • Hazard Category Code: 43
  • Safety Instruction: 36/37
  • HazardClass:IRRITANT

6-Chloropyridine-2-carboxylic acid amide Pricemore >>

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6-Chloropyridine-2-carboxylic acid amide Related Literature

Additional information on 6-Chloropyridine-2-carboxylic acid amide

Comprehensive Overview of 6-Chloropyridine-2-carboxylic acid amide (CAS No. 7059-61-2)

6-Chloropyridine-2-carboxylic acid amide (CAS No. 7059-61-2) is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. This compound, characterized by its chloropyridine backbone and carboxamide functional group, serves as a critical intermediate in synthesizing bioactive molecules. Its unique structural properties make it invaluable for developing novel heterocyclic compounds, which are increasingly sought after in drug discovery and crop protection formulations.

The growing interest in 6-Chloropyridine-2-carboxylic acid amide aligns with the surge in demand for high-purity chemical intermediates in 2024. Researchers frequently search for terms like "chloropyridine derivatives applications" or "pyridine-2-carboxamide synthesis", reflecting its relevance in modern organic chemistry. Its compatibility with cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig, further enhances its utility in constructing complex molecular architectures.

From an industrial perspective, CAS 7059-61-2 has gained attention due to its role in developing sustainable agrochemicals – a trending topic as global agriculture shifts toward eco-friendly solutions. Analytical studies confirm its stability under various pH conditions, making it suitable for formulations requiring prolonged shelf-life. Recent patents highlight its incorporation into next-generation fungicides, addressing common search queries like "chloropyridine amide fungicidal activity".

Quality control protocols for 6-Chloropyridine-2-carboxylic acid amide emphasize HPLC purity thresholds (>98%), meeting stringent requirements for pharmaceutical-grade intermediates. The compound's crystalline form exhibits excellent solubility in polar aprotic solvents – a property extensively documented in responses to searches such as "solubility of pyridine carboxamides". These characteristics facilitate its use in automated continuous-flow synthesis systems, a cutting-edge area in process chemistry.

Environmental and safety assessments reveal that 7059-61-2 demonstrates favorable biodegradation profiles compared to traditional halogenated compounds. This aligns with the industry's focus on green chemistry principles, frequently queried as "eco-friendly heterocyclic synthesis". Regulatory databases classify it as non-persistent in aquatic systems, broadening its applicability in regions with strict ecological regulations.

Innovative applications continue to emerge, particularly in material science where researchers explore its potential as a ligand for catalytic systems. The compound's ability to coordinate with transition metals responds to growing interest in "N-heterocyclic ligand design". Recent studies at MIT and ETH Zürich have demonstrated its efficacy in asymmetric catalysis – a hot topic in academic search trends.

Supply chain analytics indicate rising global demand for 6-Chloropyridine-2-carboxylic acid amide, particularly from Asian pharmaceutical hubs. This correlates with search volume spikes for "bulk chloropyridine suppliers" and "custom synthesis of pyridine amides". Manufacturers now offer multiple kilogram-scale production options with certificates of analysis tailored to GMP standards.

Future research directions may explore its derivatization for bioconjugation techniques – a trending subject in medicinal chemistry forums. The compound's compatibility with click chemistry protocols positions it as a potential building block for targeted drug delivery systems, answering frequent queries about "modular drug scaffold design". These developments underscore its enduring significance in synthetic organic chemistry.

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