Cas no 5993-95-3 (2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate)

2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate is a pyrimidine derivative with applications in pharmaceutical and chemical research. Its dihydrochloride hydrate form enhances stability and solubility, making it suitable for synthetic and biological studies. The compound features an aminomethyl functional group, which allows for further derivatization, and a methyl-substituted pyrimidine core, contributing to its reactivity in heterocyclic chemistry. The hydrate form ensures consistent handling and storage properties. This product is primarily utilized as an intermediate in the synthesis of more complex molecules, particularly in medicinal chemistry for developing potential therapeutic agents. Its well-defined structure and purity make it a reliable reagent for research applications.
2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate structure
5993-95-3 structure
Product Name:2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate
CAS No:5993-95-3
MF:C6H9N3O
MW:139.155160665512
MDL:MFCD11101119
CID:1086416
PubChem ID:135714975
Update Time:2025-10-28

2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate Chemical and Physical Properties

Names and Identifiers

    • 2-(Aminomethyl)-6-methylpyrimidin-4-ol
    • 2-(aminomethyl)-6-methyl-1H-pyrimidin-4-one,hydrochloride
    • 2-Aminomethyl-6-methyl-pyrimidin-4-ol
    • MFCD09864311
    • 5993-95-3
    • EN300-264601
    • SCHEMBL9252957
    • 4(1H)-PYRIMIDINONE, 2-(AMINOMETHYL)-6-METHYL-
    • 2-(Aminomethyl)-6-methylpyrimidin-4(3H)-one
    • VS-0259
    • SB56352
    • 2-(aminomethyl)-6-methyl-4-pyrimidinol
    • 5993-90-8
    • CHEMBL4518256
    • 2-(aminomethyl)-4-methyl-1H-pyrimidin-6-one
    • DB-324695
    • CS-0282254
    • AKOS016000067
    • AKOS012622036
    • 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate
    • MDL： MFCD11101119
    • Inchi： 1S/C6H9N3O/c1-4-2-6(10)9-5(3-7)8-4/h2H,3,7H2,1H3,(H,8,9,10)
    • InChI Key： NQUHWZJWGWWYGB-UHFFFAOYSA-N
    • SMILES： O=C1C=C(C)N=C(CN)N1

Computed Properties

  • Exact Mass: 139.074561919g/mol
  • Monoisotopic Mass: 139.074561919g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 217
  • 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: -1.3
  • Topological Polar Surface Area: 67.5?2

2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate Pricemore >>

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2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate Related Literature

Additional information on 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate

Comprehensive Guide to 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate (CAS No. 5993-95-3)

2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate (CAS No. 5993-95-3) is a specialized chemical compound with significant applications in pharmaceutical and biochemical research. This compound, often referred to as a pyrimidine derivative, is widely studied for its unique structural properties and potential therapeutic benefits. Researchers and industry professionals frequently search for pyrimidine-based compounds due to their relevance in drug development and molecular biology.

The molecular formula of 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate is C6H11N3O·2HCl·H2O, highlighting its hydrated dihydrochloride salt form. This form enhances its stability and solubility, making it suitable for various laboratory applications. The compound's aminomethyl and methylpyrimidinol functional groups contribute to its reactivity, enabling its use in synthesizing more complex molecules.

One of the trending topics in the scientific community is the exploration of heterocyclic compounds for medicinal chemistry. 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate fits into this category, as pyrimidines are key building blocks for nucleosides and nucleotides. This has led to increased interest in its potential applications, such as in the development of antiviral agents or enzyme inhibitors.

From an industrial perspective, the demand for high-purity pyrimidine derivatives is growing, particularly in the pharmaceutical sector. Companies specializing in fine chemicals and custom synthesis often seek this compound for research and development projects. Its role in peptide modification and bioconjugation techniques further underscores its versatility.

For those searching for CAS 5993-95-3 suppliers or 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate price, it is essential to consider the compound's purity and storage conditions. Proper handling ensures its longevity and effectiveness in experiments. Additionally, researchers often inquire about pyrimidine solubility and stability in aqueous solutions, which are critical for experimental success.

In summary, 2-(Aminomethyl)-6-methyl-4-pyrimidinol Dihydrochloride Hydrate (CAS No. 5993-95-3) is a valuable compound with broad applications in drug discovery and biochemical studies. Its structural features and reactivity make it a sought-after reagent in modern research. As the scientific community continues to explore heterocyclic chemistry, this compound remains a focal point for innovation and development.

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