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6-Amino-1-methyluracil

Description:


  • Nomen chemicum:6-Amino-1-methyluracil
  • CAS No.:2434-53-9
  • Formulae hypotheticae:C5 H7 N3 O2
  • Atomis computatis:5 atomi carbonis, 7 atomi Hydrogenii, 3 atomi NITROGENII, 2 atomi Oxygeni;
  • Pondus hypotheticum:141,129
  • Hs Codicis.29335990
  • Communitas Europaea (EC) Number:219-422-3
  • NSC Number:7369
  • DSSTox substantia ID:DTXSID30179076
  • Nikkaji Number:J216.075G
  • Vicimedia:Q63408603
  • ChEMBL ID:CHEMBL89725
  • Mol lima: 2434-53-9.mol
  • Product Detail

    Product Tags

    product

    Synonyma: 6-amino-1-methyl-1H-pyrimidine-2,4-dione; (7CI, 8CI); 1-Methyl-6-aminouracil;

    Chemical Property of 6-Amino-1-methyluracil

    Aspectus / Color: paene alba vel leviter beige crystallinum pulveris
    liquefactio Point: CCC ° C
    Refractivus Index: 1.548
    ● PKA:9.26±0.40(Predicta)
    PSA:80.88000
    Density: 1.339 g/cm3
    LogP: -0.76300

    ●Temp.:Repono in loco caliginoso, iners atmosphaera, locus temperatus
    ● Solubility.:Solubile sodium hydroxidum dilutum.
    ● XLogP3:-1.3
    Hydrogenium Bond Donor Comes: 2
    Hydrogenium Vinculum acceptoris comitis:3
    Rotatable vinculo comitis: 0
    ● Exacta Missa: 141.053826475
    Gravis Atom comitis: 10
    Complexity:221

    Puritas / Quality

    99%, * data a rudis instructus

    VI-Amino-I-methyluracil * data a tenui amet

    Safty Information

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

    Utilis

    ● CANONICI SMILES: CN1C(=CC(=O)NC1=O)N
    ● Usus: 6-Amino-1-methyluracil notum est effectibus inhibtoriis versus DNA glycosylasis reparandis.Notum est etiam adhiberi ut flamma retardant.6-amino-1-methyluracilo in praeparatione 1,1?-di yl-1H-spiro[pyrimido[4,5-b]quinoline-5,5?-pyrrolo[2,3-d]pyrimidine. ]-2,2?,4,4?,6?(1?H,3H,3?H,7?H,1?H)-pentaone, per reactionem cum isatin coram acido catalytico p-toluene sulfonic. .
    6-Amino-1-methyluracilum, quod Adenine vel 6-Aminopurinum notum est, compositum organicum est cum formula chemica C5H6N6O.Est pura derivatio et pars acida nucleica.Adenina una e quatuor nucleobasibus in DNA et RNA inventis, una cum cytosino, guanine et thymine (in DNA) vel uracil (in RNA).Adenine munus in processibus cellulosis crucialit ut DNA replicatio et synthesis interdum.Cum thymine (in DNA) vel uracil (in RNA) parit per compagem hydrogenii formans unum e imis paribus quae duplicem helix structuram DNA constituunt. Praeter munus suum in acida nucleica, adeninum etiam in aliis biologicis implicatur. processibus.Pars cofactorum inservit ut NADH, NADPH et FAD, quae variis enzymaticis reactionibus implicantur.Adenine adhibetur etiam in synthesi magnarum molecularum sicut ATP (triphosphate adenosina), quae notatur "energia monetarum" cellae. Adenine per varios modos obtineri potest, etiam extractio e fontibus naturalibus sicut pisces intestina vel per organica. summam.Commercium praesto est et late usus in investigationibus scientificis, applicationibus medicinae et industria pharmaceuticae. Cum adenina tractatio, norma laboratoria salutis protocolla sequenda est, incluso opportuno instrumento tutelae ac composito in area bene ventilata tractando.Gravis etiam est proprie adeninum condere ad degradationem impedire et suam stabilitatem conservare.


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