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6-Amino-1,3-dimethyluracil DMAU

Description:


  • Nomen chemicum:6-Amino-1,3-dimethyluracil DMAU
  • CAS No.:6642-31-5
  • Formulae hypotheticae:C6H9N3O2
  • Atomis computatis:6 atomi carbonis, 9 atomi Hydrogenii, 3 atomi NITROGENII, 2 atomi Oxygeni;
  • Pondus hypotheticum:155.156
  • Hs Codicis.29335990
  • Communitas Europaea (EC) Number:229-662-0
  • NSC Number:15492
  • DSSTox substantia ID:DTXSID4074350
  • Nikkaji Number:J49.015F
  • Vicimedia:Q72436408
  • Mol lima: 6642-31-5.mol
  • Product Detail

    Product Tags

    product

    Synonyma: 6-amino-1,3-dimethyluracil;

    Chemical Property of 6-Amino-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

    ● Vapor Pressure: 0.0328mmHg ad 25°C
    Punctum Point: 295 °C
    Refractivus Index: 1.55
    ● Fervens Point:23.1 °C at 760 mmHg
    ● PKA:5.17±0.70(Praedicta)
    Flash Point: 100.8 °C
    PSA:70.02000
    Density: 1.288 g/cm3
    LogP: -0.75260

    ● Repono Temp.:Store infra +30°C.
    Solubility.:6g/l
    Aqua Solubility.:7.06g/L(25 oC)
    ● XLogP3: -1.1
    Hydrogenium Bond Donor Comes: 1
    Hydrogenium Vinculum acceptoris comitis:3
    Rotatable vinculo comitis: 0
    ● Exacta Missa: 155.069476538
    Gravis Atom comitis: 11
    Complexity:246

    Puritas / Quality

    XCIX% * notitia rudis a amet

    6-Amino-1,3-dimethyluracil * data a tenui amet

    Safty Information

    Pictogram(s);product (2)Xn
    DISCRIMEN Codes: Xn
    Statements:22-36/37/38
    Salus Denunciationes: 22-26-36/37/39

    Utilis

    ● CANONICI SMILES: CN1C(=CC(=O)N(C1=O)C)N
    ● Usus: 6-Amino-1,3-dimethyluracil in synthesi pyrimidini novorum et derivationum Julius, quae valde potentiale antitumorem activitatem ostendunt.Usus est etiam ut principium materiae in synthesi pyrido-pyrimidines fusorum.
    6-Amino-1,3-dimethyluracilum est compositum chemicum cum formula hypothetica C6H8N4O.Derivatio uracil, compositio organica heterocyclica quae est pars RNA.6-Amino-1,3-dimethyluracil varias applicationes habet in campo synthesis organicae et chemiae pharmaceuticae.Adhiberi potest ut scandalum aedificium ad synthesim compositorum biologice activae, sicut medicamenta pharmaceutica et agrochemicals. Haec compositio coetus amino (NH2) et duo coetus yl methyl (-CH3) diversis atomis carbonis in uracil anulo adiuncti sunt.Praesentia coetus amino magis reactivum facit ad diversas reactiones chemicas, inclusas substitutionem et condensationem reactiones. In chemia medicinali, 6-Amino-1,3-dimethyluracil, uti potest ut principium materiae ad synthesim medicamentorum uracil-fundatorum; quae varias biologicas habent actiones.Potest etiam adhiberi ut clavis media in synthesi nucleosidum et nucleotidum, quae necessariae sunt structurae caudices pro DNA et RNA synthesi. Ceterum haec compositio adhiberi potest in analyticis methodis ad detectionem et quantitatem derivationum uracilis. Exempla biologica. Plus, 6-Amino-1,3-dimethyluracil est momenti compositum quod invenit applicationes in synthesi organica et chemia pharmaceutica, fungens munus vitale in evolutione compositionum biologicarum activarum et methodorum analyticorum in campo biologiae hypotheticae.


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