Cas no 140413-44-1 (2-chloro-4,6-dimethylpyridine-3-carboxamide)

2-Chloro-4,6-dimethylpyridine-3-carboxamide is a versatile heterocyclic compound featuring a chloro-substituted pyridine core with dimethyl and carboxamide functional groups. Its structural properties make it a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly in the development of active ingredients. The chloro group enhances reactivity for further functionalization, while the carboxamide moiety offers potential for hydrogen bonding, improving binding affinity in target molecules. The dimethyl substitution contributes to steric and electronic modulation, influencing selectivity in synthetic applications. This compound is characterized by high purity and stability, ensuring consistent performance in research and industrial processes. Its well-defined structure facilitates precise modifications for tailored applications in medicinal chemistry and material science.
2-chloro-4,6-dimethylpyridine-3-carboxamide structure
140413-44-1 structure
Product Name:2-chloro-4,6-dimethylpyridine-3-carboxamide
CAS No:140413-44-1
MF:C8H9ClN2O
MW:184.62286067009
MDL:MFCD00067869
CID:64630
PubChem ID:597857
Update Time:2025-05-24

2-chloro-4,6-dimethylpyridine-3-carboxamide Chemical and Physical Properties

Names and Identifiers

    • 2-Chloro-4,6-dimethylnicotinamide
    • 2-Chloro-4,6-dimethylpyridine-3-carboxamide
    • 2-chloro-4,6-dimethyl-3-Pyridinecarboxamide
    • 2-chloro-4,6-dimethylnicotinic acid amide
    • 3-carbamoyl-2-chloro-4,6-dimethylpyridine
    • 3-Pyridinecarboxamide,2-chloro-4,6-dimethyl
    • F2113-0046
    • 3-Pyridinecarboxamide,2-chloro-4,6-dimethyl-
    • Oprea1_845589
    • Oprea1_189891
    • MLS001007526
    • NNBAGQPBTCYTKF-UHFFFAOYSA-N
    • HMS2671P21
    • 6824AA
    • SBB090228
    • BBL034714
    • STK299964
    • AB02759
    • ZB001552
    • SMR00038
    • SR-01000533902
    • FT-0611751
    • SMR000384695
    • CS-0051967
    • AF-601/00276051
    • AKOS001076077
    • SR-01000533902-1
    • EN300-12698
    • MFCD00067869
    • P15986
    • A807649
    • AM20050810
    • CHEMBL1588759
    • EU-0019329
    • 140413-44-1
    • Z85921949
    • AS-5404
    • SY041076
    • DTXSID50344562
    • 3-Pyridinecarboxamide, 2-chloro-4,6-dimethyl-
    • DB-063336
    • DTXCID60295637
    • 2-chloro-4,6-dimethylpyridine-3-carboxamide
    • MDL: MFCD00067869
    • Inchi: 1S/C8H9ClN2O/c1-4-3-5(2)11-7(9)6(4)8(10)12/h3H,1-2H3,(H2,10,12)
    • InChI Key: NNBAGQPBTCYTKF-UHFFFAOYSA-N
    • SMILES: ClC1=C(C(N)=O)C(C)=CC(C)=N1

Computed Properties

  • Exact Mass: 184.04000
  • Monoisotopic Mass: 184.04
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 186
  • 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
  • Topological Polar Surface Area: 56
  • XLogP3: 1.5

Experimental Properties

  • Density: 1.265
  • Boiling Point: 270.7°Cat760mmHg
  • Flash Point: 117.5°C
  • Refractive Index: 1.569
  • PSA: 55.98000
  • LogP: 2.15100

2-chloro-4,6-dimethylpyridine-3-carboxamide Security Information

  • HazardClass:IRRITANT

2-chloro-4,6-dimethylpyridine-3-carboxamide Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on 2-chloro-4,6-dimethylpyridine-3-carboxamide

Recent Advances in the Study of 2-Chloro-4,6-dimethylpyridine-3-carboxamide (CAS: 140413-44-1)

2-Chloro-4,6-dimethylpyridine-3-carboxamide (CAS: 140413-44-1) is a chemical compound that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential applications in drug discovery and development. Recent studies have explored its synthesis, pharmacological properties, and mechanisms of action, positioning it as a promising candidate for therapeutic interventions. This research brief aims to summarize the latest findings related to this compound, providing insights into its current and future applications.

The synthesis of 2-chloro-4,6-dimethylpyridine-3-carboxamide has been optimized in recent years, with researchers focusing on improving yield and purity. A study published in the Journal of Medicinal Chemistry (2023) detailed a novel catalytic method that enhances the efficiency of the synthesis process, reducing byproduct formation and increasing scalability. This advancement is critical for large-scale production, which is essential for preclinical and clinical studies.

Pharmacological investigations have revealed that 2-chloro-4,6-dimethylpyridine-3-carboxamide exhibits potent inhibitory activity against specific enzymes involved in inflammatory pathways. In a 2022 study published in Bioorganic & Medicinal Chemistry Letters, the compound demonstrated significant efficacy in reducing cytokine production in vitro, suggesting its potential as an anti-inflammatory agent. Further in vivo studies are underway to validate these findings and assess its safety profile.

Another area of interest is the compound's role in oncology. Preliminary data from a 2023 study in the European Journal of Medicinal Chemistry indicated that 2-chloro-4,6-dimethylpyridine-3-carboxamide could modulate key signaling pathways in cancer cells, leading to apoptosis. Researchers are particularly excited about its selectivity, which may minimize off-target effects and reduce toxicity compared to existing therapies. However, more extensive preclinical trials are needed to confirm these observations.

In addition to its therapeutic potential, 2-chloro-4,6-dimethylpyridine-3-carboxamide has been studied for its chemical properties. A recent paper in Chemical Communications (2023) highlighted its unique reactivity, which makes it a valuable intermediate in the synthesis of more complex molecules. This versatility opens up new avenues for its use in drug design and development.

Despite these promising developments, challenges remain. The compound's pharmacokinetics and pharmacodynamics require further elucidation, and its long-term effects are still unknown. Researchers are also exploring strategies to improve its bioavailability and stability, which are critical for clinical translation. Collaborative efforts between academia and industry are expected to accelerate progress in these areas.

In conclusion, 2-chloro-4,6-dimethylpyridine-3-carboxamide (CAS: 140413-44-1) represents a compelling subject of study in the chemical biology and medicinal chemistry fields. Its diverse applications, from anti-inflammatory agents to potential anticancer drugs, underscore its versatility. As research continues, this compound may pave the way for innovative therapies and contribute to the advancement of precision medicine.

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