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2,4-Diamino-6-hydroxypyrimidine

Description:


  • Product nomen:2,4-Diamino-6-hydroxypyrimidine
  • Synonyma:TIMTEC-BB SBB004252;2,4-DIAMINOPYRIMIDIN-6-OL;2,4-DIAMINO-6-HYDROXYPYRIMIDINE;2,4-DIAMINO-6-PYRIMIDINOL;2,4-DIAMINO-6(1H)-PYRIMIDINONE; 6-DIAMINO-4-PYRIMIDINOL;2,6-DIAMINO-4-PYRIMIDINONE;2,6-DIAMINOPYRIMIDIN-4-OL
  • CAS;56-06-4
  • MF:C4H6N4O
  • MW:126.12
  • EINECS:200-254-4
  • Categoria:Pyrimidines;exstructiones;PYRIMIDINE;C4 ad C5;Chemica Synthesis; Heterocyclica Aedificium Cuneos; APIs & Medium; Pyridines, Pyrimidines, Purines & Pteredines;Amines Chemical;13C & 2H Sugars;Amines;Bases & Reagents; Heterocycles; & Derivationes, bc0001
  • Mol fasciculi:56-06-4.mol
  • Product Detail

    Product Tags

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    Hydroxypyrimidine Chemical Properties

    Liquescens punctum 285-286 °C (decl.)
    Ferveret 234.22°C (aestimatio aspera)
    density 1.3659 (aestimatio aspera)
    refractivus index 1.7990 (aestima)
    repono temp. Serva in caliginoso loco, atmosphaera Inert, locus temperatus
    solubility DMSO (paulo), Methanol (paulo)
    pka 10.61±0.50 (Praedicta)
    forma Pulchra crystallina pulveris
    color Alba ad crepito
    Sensitiva lux Sensitiva
    Merck 14,2981
    BRN 125006
    InChIKey SWELIMKTDYHAOY-UHFFFAOYSA-N
    CAS Reference 56-06-4 (CAS Reference)
    NIST Chemia Reference 4(1H)-pyrimidinone, 2,6-diamino-(56-06-4)
    EPA Substantia Registry System 2,6-Diamino-4(1H)-pyrimidinone (56-06-4)

    Hydroxypyrimidine Product Description

    2,4-Diamino-6-hydroxypyrimidine est compositum chemicum cum formula hypothetica C4H6N4O.Compositum est organicum familiae pyrimidinis pertinens.Compositum pyrimidinem structuram anuli habet, duo coetus amino (NH2) conexi cum 2-positione et 4-positione, et globus hydroxylus (OH) cum 6-positione connexus est.Chemica structura exprimi potest ut: Ammonia ||H--C--C--C--N--C--C--NH2 ||oh 2,4-Diamino-6-hydroxypyrimidine varias applicationes in pharmaceutica industria habet.Medium magni momenti est in synthesi multarum medicamentorum, in quibus medicinae antiviralis et antitumor est.Usus est etiam ad plura analoga nucleotide in pharmaceutica inquisitione adhibita.

    Praeter medicamenta medicamenta, 2,4-diamino-6-hydroxypyrimidine medicamenta in agrochemicals adhibetur.Clavis est ingrediens in synthesi plantae incrementi regulatores et fungicides.Magni interest ut propriam salutem protocollo sequantur cum adhibita 2,4-diamino-6-hydroxypyrimidine.Cum inritamentum chemicum generetur, cura et adaequata instrumenta tutelae personalis tractari debet ad contactum directum vitandum.

    In summa, 2,4-diamino-6-hydroxypyrimidine compositum est organicum cum applicationibus in agris pharmaceuticis et agriculturae.Eius structura chemica eam utilem facit ut medium in synthesi pharmaceuticae et incrementi regulatores plantandi.

    Salus Information

    Periculum Codes Xi
    Periculum Denunciationes 36/37/38
    Salus Denunciationes 22-24/25-36-26
    WGK Germania 3
    Aleam Nota Irritant
    TSCA Ita
    HS Code* 29335995

    Hydroxypyrimidine Synthesis Synthesis

    Descriptio 2,4-Diamino-6-hydroxypyrimidinum (DAHP) est selectivum, specificum inhibitoris GTP cyclohydrolasi I, gradatim limitans pro synthesi novo pterin.In cellulis HUVEC, IC50inhibitionis BH*4biosynthesis est circiter 0,3 mM.DAHP adhiberi potest ad nullas productiones efficaciter angustas in pluribus cellulis speciebus.
    Chemical Properties Solidus albus
    usus 2,4-Diamino-6-hydroxypyrimidinum (DAHP) est selectivum, specificum inhibitoris GTP cyclohydrolasi I, gradatim limitans pro synthesi novo pterin.In cellulis HUVEC, IC50 in inhibitionis biosynthesis BH4 est circiter 0.3 mM.DAHP adhiberi potest ut efficaciter nullum productionem impediat in pluribus cellulis speciebus.[Cayman Chemical]
    usus Stat in principio cascade enzyme-catalytici qui cum hoc carbohydrato septem-carbo incipit et cum amino amino aromatico phenylalanino, tyrosino et tryptophano terminatur.
    usus 2,4-Diamino-6-hydroxypyrimidinum (cas# 56-06-4) compositum utile est in synthesi organica.
    Purificationis Methodi Recrystallises ab H2O.[Beilstein 25 III/IV 3642.]

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