Cas no 4763-53-5 (4,5-Dimethoxypyrimidin-2-amine)

4,5-Dimethoxypyrimidin-2-amine is a pyrimidine derivative characterized by its dimethoxy substitution at the 4 and 5 positions and an amino group at the 2 position. This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structural features make it valuable for constructing heterocyclic frameworks, with applications in medicinal chemistry for designing kinase inhibitors and other bioactive molecules. The dimethoxy groups enhance solubility and stability, while the amino group provides a reactive site for further functionalization. The compound is typically handled under standard laboratory conditions, ensuring compatibility with a range of synthetic protocols.
4,5-Dimethoxypyrimidin-2-amine structure
4763-53-5 structure
Product Name:4,5-Dimethoxypyrimidin-2-amine
CAS No:4763-53-5
MF:C6H9N3O2
MW:155.154560804367
MDL:MFCD09027684
CID:931148
PubChem ID:12988104
Update Time:2025-10-30

4,5-Dimethoxypyrimidin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 4,5-Dimethoxypyrimidin-2-amine
    • 4,5-dimethoxy-pyrimidin-2-ylamine
    • 2-Amino-4,5-dimethoxy-pyrimidin
    • 2-amino-5,6-dimethoxypyrimidine
    • 2-Pyridinecarboxaldehyde,4,5-dimethoxy
    • 4,5-Dimethoxy-2-formylpyridin
    • 4,5-dimethoxypicolinaldehyde
    • 4,5-dimethoxypyridin-2-aldehyde
    • 4,5-dimethoxy-pyridine-2-carbaldehyde
    • A827286
    • 2-amino-4,5-dimethoxypyrimidine
    • SCHEMBL2897696
    • 4,5-dimethoxy-2-pyrimidinamine
    • SY268230
    • FNCVECQZXCCHJM-UHFFFAOYSA-N
    • SB56000
    • AKOS006290051
    • MFCD09027684
    • 4763-53-5
    • DTXSID80514433
    • MDL: MFCD09027684
    • Inchi: 1S/C6H9N3O2/c1-10-4-3-8-6(7)9-5(4)11-2/h3H,1-2H3,(H2,7,8,9)
    • InChI Key: FNCVECQZXCCHJM-UHFFFAOYSA-N
    • SMILES: O(C)C1=CN=C(N)N=C1OC

Computed Properties

  • Exact Mass: 155.06900
  • Monoisotopic Mass: 155.069476538g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 122
  • 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: 0.1
  • Topological Polar Surface Area: 70.3?2

Experimental Properties

  • PSA: 70.26000
  • LogP: 0.65720

4,5-Dimethoxypyrimidin-2-amine Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the 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:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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4,5-Dimethoxypyrimidin-2-amine Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:4763-53-5)4,5-Dimethoxypyrimidin-2-amine
Order Number:A827286
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:11
Price ($):1243.0

Additional information on 4,5-Dimethoxypyrimidin-2-amine

4,5-Dimethoxypyrimidin-2-amine (CAS No. 4763-53-5): A Comprehensive Overview

4,5-Dimethoxypyrimidin-2-amine, also known by its CAS registry number 4763-53-5, is a heterocyclic organic compound that has garnered significant attention in the fields of chemistry, pharmacology, and materials science. This compound belongs to the pyrimidine family, a class of six-membered aromatic rings with two nitrogen atoms at positions 1 and 3. The presence of methoxy groups at positions 4 and 5, along with an amine group at position 2, imparts unique chemical and biological properties to this molecule.

The synthesis of 4,5-Dimethoxypyrimidin-2-amine is typically achieved through multi-step organic reactions. One common approach involves the condensation of aldehydes or ketones with ammonia or primary amines, followed by cyclization to form the pyrimidine ring. The introduction of methoxy groups is often accomplished via nucleophilic substitution or coupling reactions. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing production costs and environmental impact.

4,5-Dimethoxypyrimidin-2-amine exhibits a wide range of applications across various industries. In the pharmaceutical sector, it serves as an intermediate in the synthesis of bioactive compounds targeting diseases such as cancer and inflammation. For instance, researchers have reported its use in designing inhibitors for kinases and other enzymes involved in disease progression. The compound's ability to modulate cellular signaling pathways makes it a valuable tool in drug discovery.

In materials science, 4,5-Dimethoxypyrimidin-2-amine has been explored as a building block for advanced materials such as coordination polymers and metal-organic frameworks (MOFs). Its nitrogen-rich structure facilitates strong interactions with metal ions, leading to highly porous and stable materials with potential applications in gas storage and catalysis. Recent studies have demonstrated its role in creating MOFs with exceptional adsorption capacities for gases like CO? and CH?.

The biological activity of 4,5-Dimethoxypyrimidin-2-amine is another area of intense research interest. Preclinical studies have shown that this compound possesses anti-inflammatory and antioxidant properties, making it a promising candidate for treating conditions like neurodegenerative diseases and cardiovascular disorders. Additionally, its ability to inhibit certain bacterial enzymes suggests potential applications in antimicrobial therapy.

From an environmental perspective, 4,5-Dimethoxypyrimidin-2-amine has been studied for its role in green chemistry processes. Its use as a catalyst or reagent in sustainable chemical transformations aligns with global efforts to reduce waste and energy consumption in industrial settings. Recent breakthroughs include its application in asymmetric synthesis reactions that minimize byproduct formation.

In conclusion, 4,5-Dimethoxypyrimidin-2-amine (CAS No. 4763-53-5) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical structure, coupled with ongoing advancements in synthesis and application development, ensures its continued relevance in scientific research and industrial innovation.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:4763-53-5)4,5-Dimethoxypyrimidin-2-amine
A827286
Purity:99%
Quantity:1g
Price ($):1243.0
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