Cas no 57639-19-7 (4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine)

4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine is a heterocyclic organic compound featuring a triazine core substituted with chloro and dimethylamino functional groups. This structure imparts reactivity suitable for applications in agrochemical and pharmaceutical synthesis, particularly as an intermediate in the production of herbicides and fungicides. Its chloro group enables nucleophilic substitution reactions, while the dimethylamino moiety enhances solubility and stability in various formulations. The compound’s high purity and consistent performance make it a reliable choice for research and industrial processes requiring precise molecular modifications. Proper handling and storage are recommended due to its potential sensitivity to moisture and light.
4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine structure
57639-19-7 structure
Product Name:4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine
CAS No:57639-19-7
MF:C5H7ClN4
MW:158.58887887001
MDL:MFCD20661905
CID:4653301
PubChem ID:12237262
Update Time:2025-06-13

4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine
    • 1,3,5-Triazin-2-amine, 4-chloro-N,6-dimethyl-
    • SB73400
    • W11899
    • 4-chloro-2-methyl-6-methylamino-1,3,5-triazine
    • N-(4-chloro-6-methyl-1,2-dihydro-1,3,5-triazin-2-ylidene)methanamine
    • AKOS037646120
    • CS-0035496
    • 57639-19-7
    • SCHEMBL2678562
    • AKOS027255735
    • MFCD20661905
    • AS-66719
    • DTXSID101260678
    • OOJFLTDNAJUBKR-UHFFFAOYSA-N
    • MDL: MFCD20661905
    • Inchi: 1S/C5H7ClN4/c1-3-8-4(6)10-5(7-2)9-3/h1-2H3,(H,7,8,9,10)
    • InChI Key: OOJFLTDNAJUBKR-UHFFFAOYSA-N
    • SMILES: ClC1N=C(C)N=C(N=1)NC

Computed Properties

  • Exact Mass: 158.0359239g/mol
  • Monoisotopic Mass: 158.0359239g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 110
  • 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: 1.7
  • Topological Polar Surface Area: 50.7

4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine Pricemore >>

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Additional information on 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine

Research Brief on 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine (CAS: 57639-19-7): Recent Advances and Applications

4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine (CAS: 57639-19-7) is a triazine derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its versatile applications in drug discovery and agrochemical development. Recent studies have explored its potential as a key intermediate in the synthesis of novel bioactive compounds, particularly in the development of herbicides and antimicrobial agents. This research brief aims to summarize the latest findings related to this compound, highlighting its chemical properties, biological activities, and potential industrial applications.

A study published in the Journal of Agricultural and Food Chemistry (2023) investigated the herbicidal efficacy of 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine derivatives. The research demonstrated that these compounds exhibit strong inhibitory effects on the growth of broadleaf weeds, with a mechanism of action involving the disruption of photosynthesis. The study also highlighted the compound's favorable environmental profile, as it degrades rapidly in soil, minimizing long-term ecological impact. These findings suggest its potential as a sustainable alternative to traditional herbicides.

In the pharmaceutical domain, recent research has focused on the antimicrobial properties of 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine. A 2024 study in Bioorganic & Medicinal Chemistry Letters reported that structural modifications of this compound led to derivatives with potent activity against drug-resistant bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA). The researchers identified that the chloro and dimethylamino groups play crucial roles in binding to bacterial target proteins, offering insights for further structure-activity relationship (SAR) studies.

From a chemical synthesis perspective, advancements have been made in the production of 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine. A recent patent (WO2023124567) disclosed an improved synthetic route that enhances yield and purity while reducing hazardous byproducts. This development is particularly significant for industrial-scale production, addressing previous challenges in the compound's manufacturing process.

Looking forward, the unique structural features of 4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amine continue to inspire novel applications. Current research directions include its potential as a building block for metal-organic frameworks (MOFs) with applications in drug delivery, as well as investigations into its use as a corrosion inhibitor in industrial settings. The compound's versatility and the ongoing research interest suggest it will remain an important focus in chemical and pharmaceutical development for years to come.

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