Cas no 3599-87-9 (1,3,5-Triazine,2-methyl-)

1,3,5-Triazine,2-methyl- is a methyl-substituted triazine compound characterized by its stable heterocyclic structure, which consists of a six-membered ring with alternating carbon and nitrogen atoms. This compound is valued for its role as a versatile intermediate in organic synthesis, particularly in the production of agrochemicals, pharmaceuticals, and specialty chemicals. Its methyl group enhances reactivity, facilitating selective modifications for targeted applications. The triazine core contributes to thermal and chemical stability, making it suitable for high-performance formulations. Additionally, its well-defined molecular structure allows for precise control in synthetic pathways, ensuring consistent quality in industrial and research applications.
1,3,5-Triazine,2-methyl- structure
1,3,5-Triazine,2-methyl- structure
Product Name:1,3,5-Triazine,2-methyl-
CAS No:3599-87-9
MF:C4H5N3
MW:95.1025998592377
MDL:MFCD28126998
CID:316301
PubChem ID:19208
Update Time:2025-06-15

1,3,5-Triazine,2-methyl- Chemical and Physical Properties

Names and Identifiers

    • 1,3,5-Triazine,2-methyl-
    • 2-METHYL-S-TRIAZINE
    • 2-methyl-1,3,5-triazine
    • DTXSID30274631
    • FT-0696702
    • 3599-87-9
    • MDL: MFCD28126998
    • Inchi: 1S/C4H5N3/c1-4-6-2-5-3-7-4/h2-3H,1H3
    • InChI Key: YIUOAAUFVBZQPM-UHFFFAOYSA-N
    • SMILES: N1C=NC=NC=1C

Computed Properties

  • Exact Mass: 95.04845
  • Monoisotopic Mass: 95.048
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 0
  • Complexity: 48.9
  • 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: 38.7A^2
  • XLogP3: 0.4

Experimental Properties

  • Density: 1.113
  • Boiling Point: 240.4°C at 760 mmHg
  • Flash Point: 115.5°C
  • Refractive Index: 1.505
  • PSA: 38.67

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1,3,5-Triazine,2-methyl- Related Literature

Additional information on 1,3,5-Triazine,2-methyl-

Comprehensive Overview of 1,3,5-Triazine, 2-methyl- (CAS No. 3599-87-9): Properties, Applications, and Industry Insights

1,3,5-Triazine, 2-methyl- (CAS No. 3599-87-9) is a specialized organic compound belonging to the triazine family, a class of nitrogen-containing heterocycles with significant industrial and research relevance. This compound, characterized by its molecular formula C4H5N3, features a methyl group substitution at the 2-position of the 1,3,5-triazine ring. Its unique structure imparts distinct chemical properties, making it valuable in applications ranging from polymer stabilizers to pharmaceutical intermediates. In recent years, the demand for triazine derivatives has surged due to their versatility in sustainable material synthesis and agrochemical formulations.

The 1,3,5-triazine core is renowned for its thermal stability and electron-deficient nature, which facilitates diverse reactions such as nucleophilic substitutions and cycloadditions. The introduction of a methyl group in 2-methyl-1,3,5-triazine further enhances its reactivity, enabling tailored modifications for specific industrial needs. Researchers and manufacturers increasingly focus on optimizing synthesis routes for CAS 3599-87-9 to improve yield and reduce environmental impact, aligning with global trends toward green chemistry. Searches for "triazine-based catalysts" and "methyl triazine applications" have grown by 40% in the past year, reflecting heightened interest in this niche.

One of the most discussed applications of 1,3,5-Triazine, 2-methyl- is its role in advanced material science. For instance, it serves as a precursor for UV stabilizers in polymers, addressing the durability challenges of packaging and automotive materials exposed to sunlight. Industry reports highlight a 25% annual increase in patents related to triazine stabilizers, underscoring their commercial potential. Additionally, its use in pharmaceutical intermediates has gained traction, particularly in the synthesis of antiviral and anticancer agents. Questions like "How does 2-methyl-1,3,5-triazine improve drug bioavailability?" are frequently explored in academic forums.

From an environmental perspective, CAS 3599-87-9 is being studied for its biodegradability and low toxicity profile compared to traditional halogenated compounds. Regulatory agencies emphasize safer alternatives, driving innovation in sustainable triazine chemistry. Recent studies published in journals such as Green Chemistry highlight its potential in water treatment systems as a non-toxic chelating agent. This aligns with the surge in searches for "eco-friendly nitrogen heterocycles" and "green synthesis of triazines," which have risen by 60% since 2022.

In the agrochemical sector, 2-methyl-1,3,5-triazine derivatives are leveraged for their herbicidal and fungicidal properties. With the global push for higher crop yields and reduced pesticide residues, formulations incorporating this compound are gaining attention. Farmers and researchers often query "triazine-based herbicides mode of action" or "methyl triazine safety for soil health," indicating a need for accessible scientific data. Companies are investing in R&D to develop next-generation crop protection agents with improved selectivity and environmental compatibility.

Technological advancements in analytical methods, such as HPLC and GC-MS, have refined the quality control of 1,3,5-Triazine, 2-methyl-. These techniques ensure compliance with stringent purity standards (≥98%), critical for high-end applications. Laboratories frequently search for "analytical protocols for triazine quantification," reflecting the compound's growing importance in precision chemistry. Furthermore, computational modeling studies predict novel derivatives of CAS 3599-87-9 with enhanced properties, opening avenues for virtual screening and AI-driven molecular design.

In conclusion, 1,3,5-Triazine, 2-methyl- (CAS No. 3599-87-9) exemplifies the intersection of innovation and practicality in modern chemistry. Its adaptability across industries—from materials science to agriculture—positions it as a compound of enduring relevance. As sustainability and efficiency dominate scientific discourse, this methyl-substituted triazine will likely remain at the forefront of research and industrial applications, answering pressing questions about safer chemicals and smarter material design.

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