Cas no 175204-67-8 (4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol)

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol is a heterocyclic compound featuring a triazine core substituted with an amino group, a cyclopropyl moiety, and a hydroxyl group. This structure imparts unique reactivity, making it a valuable intermediate in organic synthesis and agrochemical applications. The cyclopropyl group enhances steric and electronic properties, while the amino and hydroxyl functionalities offer sites for further derivatization. Its stability under varied conditions and compatibility with diverse reaction pathways make it suitable for developing specialized chemicals, including potential herbicides or pharmaceutical precursors. The compound’s well-defined molecular architecture ensures consistent performance in research and industrial processes.
4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol structure
175204-67-8 structure
Product Name:4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol
CAS No:175204-67-8
MF:C6H8N4O
MW:152.153920173645
CID:133961
PubChem ID:135410099
Update Time:2025-05-20

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol Chemical and Physical Properties

Names and Identifiers

    • 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol
    • 1,3,5-Triazin-2(1H)-one,6-amino-4-cyclopropyl-
    • 2-amino-6-cyclopropyl-1H-1,3,5-triazin-4-one
    • 2-AMINO-4-CYCLOPROPYL-6-HYDROXY-1,3,5-TRIAZINE
    • HMS1445A15
    • BUTTPARK 43\57-29
    • 1,3,5-Triazin-2(1H)-one,4-amino-6-cyclopropyl-(9CI)
    • CS-0216338
    • FT-0617537
    • Maybridge3_004943
    • IDI1_016330
    • DTXSID10381938
    • MFCD00052766
    • 4-AMINO-6-CYCLOPROPYL-1H-1,3,5-TRIAZIN-2-ONE
    • SB73510
    • Z1255383141
    • 175204-67-8
    • AKOS015908880
    • Oprea1_182419
    • SCHEMBL13833298
    • 1,3,5-Triazin-2(1H)-one, 6-amino-4-cyclopropyl-
    • EN300-399908
    • AKOS026731020
    • Inchi: 1S/C6H8N4O/c7-5-8-4(3-1-2-3)9-6(11)10-5/h3H,1-2H2,(H3,7,8,9,10,11)
    • InChI Key: KZULJRIAAGBPGO-UHFFFAOYSA-N
    • SMILES: O=C1N=C(N)N=C(C2CC2)N1

Computed Properties

  • Exact Mass: 152.07000
  • Monoisotopic Mass: 152.07
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 264
  • 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: -0.8
  • Topological Polar Surface Area: 79.8?2

Experimental Properties

  • Density: 1.89
  • Boiling Point: 285.1°C at 760 mmHg
  • Flash Point: 126.2°C
  • Refractive Index: 1.89
  • PSA: 84.92000
  • LogP: 0.61800

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol Security Information

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol Pricemore >>

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Additional information on 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol: A Comprehensive Overview

4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol, identified by the CAS number 175204-67-8, is a compound of significant interest in the fields of organic chemistry and materials science. This compound is notable for its unique structure and potential applications in various industries. The molecule consists of a triazine ring with an amino group at position 4 and a cyclopropyl group at position 6, along with a hydroxyl group at position 2. This combination of functional groups imparts the compound with distinctive chemical properties that make it a valuable subject for research and development.

The synthesis of 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol involves a series of carefully controlled reactions that ensure the formation of the desired triazine ring structure. Recent advancements in synthetic methodologies have enabled researchers to optimize the production process, leading to higher yields and improved purity levels. The use of catalytic systems and green chemistry principles has further enhanced the sustainability of this synthesis pathway.

One of the most promising applications of this compound lies in its potential as a precursor for advanced materials. The triazine ring structure is known to exhibit excellent thermal stability and mechanical properties, making it suitable for applications in high-performance polymers and composites. Researchers have explored the incorporation of 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol into polymeric matrices to enhance their durability and resistance to environmental factors.

In addition to its material science applications, this compound has also garnered attention in the pharmaceutical industry. The presence of an amino group and a hydroxyl group provides opportunities for functionalization, enabling the development of bioactive molecules with potential therapeutic effects. Recent studies have investigated the ability of derivatives of this compound to interact with specific biological targets, such as enzymes and receptors, opening new avenues for drug discovery.

The cyclopropyl group in 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol introduces strain into the molecule, which can be harnessed to create reactive intermediates for various chemical transformations. This property has led to its use as a building block in organic synthesis, where it serves as a versatile platform for constructing complex molecular architectures.

From an environmental perspective, understanding the behavior and fate of 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol in different ecosystems is crucial for assessing its potential impact on human health and the environment. Recent studies have focused on evaluating its biodegradability and toxicity under various conditions, providing valuable insights into its safe handling and disposal.

In conclusion, 4-Amino-6-cyclopropyl-1,3,5-triazin-2-ol, with its unique structure and diverse functional groups, continues to be a focal point for scientific exploration and innovation across multiple disciplines. Its potential applications span from advanced materials to pharmaceuticals, underscoring its importance in modern chemical research.

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