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II-amino-V, Methylpytridine, Cas No. 1603-41-4

Short description:

  • Donec nomen: II-amino-V, methylpytridine
  • Cas No.:1603-41-4
  • Molecular Formula: C6H8N2
  • Computatis Atoms: VI Carbon Atoms, VIII Hydrogenium Atoms, II NITROGENIUM atomi,
  • M. pondus 108.143
  • HS Code.:29339999
  • Europae Community (EC) Number: 216-503-5
  • NSC Number: 96444,1489
  • UNII: 8um54t43wt
  • Dsstox substantia ID: Dtxsid4029220
  • Nikkaji Number: J31.383A
  • Wikidata: Q27271041
  • Pharos Ligand ID: 8Xpzjhz9g3xy
  • Chembl ID: Chembl61990

  • Chemical nomen:II-amino-V, methylpytridine
  • CAS non.:1603-41-4
  • Molecular formula:C6h8n2
  • Computatis atomorum:VI Carbon Atoms, VIII Hydrogenium Atoms, II NITROGENIUM Atoms:
  • Molecular pondus:108.143
  • HS Code.:29333999
  • Europae Community (EC) Number:216-503-5
  • NSC numero:96444,1489
  • UNII:8um54t43wt
  • Dsstox substantia ID:DTXSID4029220
  • Nikkaji Number:J31.383a
  • Wikidata:Q27271041
  • Pharos Ligand ID:8xpzjhz9g3xy
  • Chembl ID:Chembl61990
  • Mol file: 1603-41-4.mol
  • Product Detail

    Product Tags

    Product (II)

    Synonyma: (III-trifluoromethylpytridin-II-yl) Amine, 3- (trifluoromethyl) -2, Pyridinamine;

    Chemical res II-amino-V, methylpytridine

    ● species / color: albus aut flavo crystal
    ● Vapor pressura: 0.0794MMMHG ad XXV ° C
    ● Melting Point: 76-77 ° C (Lit.)
    ● Refractive Index: 1,524-1,528
    ● ferventis Point: 226,999 ° C ad DCCLX Mmhg
    ● Pka: Pk1: 7.22 (I) (XXV ° F)
    ● Flash Point: 110,863 ° C
    ● Psalm: 38.91000
    ● Density: 1.068 G / CM3
    ● Listp: 1.55340

    ● repono temp.refrigerator
    ● sensitive.:hygroscopic
    ● Solubility.:1000G/l
    ● Xlogp3: I
    ● hydrogenii vinculum donator comitem: I
    ● Hydrogenii Bond Reformes comitem: II
    ● Rotatable vinculum comitem: 0
    ● Missam exact: 108.068748264
    ● Gravis Atom comitem: VIII
    ● Complexity: 72.9

    Puritas / Quality

    XCIX% * data a rudis Suppliers

    II-amino-V, Methylpyridine XCVIII% * data ex Reagent Suppliers

    Notitia safty

    ● Hazart Codes: T, XII
    ● statements: XXIII / XXIV / 25-36 / XXXVII / 38-25
    ● Salutis statements: 26-36 / XXXVII / 39-45-37 / 39-28a

    Utilis

    ● canonical ridet: cc1 = CN = c (c = C1) n
    ● utitur: II-amino-V, methylpyridine est chemical compositis cum mocecular formula c6h8n2. It is a pyridine derivative that contains an amino group (-NH2) and a methyl group (-CH3) attached to the pyridine ring.This compound is often used as a building block or intermediate in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and dyes. Potest etiam adhiberi precursor ad synthesim heterocyclic compositis cum quis eget compositis, est momenti ad sequi propriis salus protocols et consulere certa fontes cum opus cum aut tractantem II-amino-V, Methylpyridine.

    Detailed introductio

    II-amino-V, methylpytridine, Etiam notum est V, Methyl-II-aminopyridine vel amp, est chemical compositis cum mocecular formula c₆h₈n₂. Pertinet Pyridiana familia organicum componit et ex pyridine anulus substituatur cum amino coetus (-nh₂) ad II-situ et methyl coetus (-ch₃) ad V-situ.
    Hoc compositis est colore pallide flavum liquidum cum proprium odorem. Est solutum in organicis solvents ut ethanol et aether sed limitata solubility in aquis.
    II, amino-V, methylpyridine invenit applicationem in variis agris. Hoc est communiter ut a aedificium obstructionum in organicum synthesis, praecipue in pharmaceutical industria, ad synthesis de variis componit cum biologicum actio. Et versatile structuram concedit ad introductionem diversis eget coetus, faciens eam a mediocriter in productione pharmaceuticals, agrochemicals et dyes.
    Ob suam basic proprietatibus, II-amino-V, methylpyridine potest etiam esse sicut catalyst in variis eget profectae. Potest agere ut Ligand in coordinatione elit et forma complexa cum metallum ions.
    Aliquam sit amet est tractare hoc compositis cum caute, ut sit noxia, si absorbuit, haustus, aut absorbuit per cutem. Propriis tutela apparatu et tractantem procedendi debet sequi cum operantes cum II-amino-V, methylpyridine.

    Applicatio

    Hic sunt quaedam specifica applications de II-amino-V, methylpyridine:
    Pharmaceutical Industry:II-amino-V, Methylpyridine adhibetur ut a versatile medium ad synthesim variis pharmaceutical componit. Potest adhiberi ut a aedificium obstructionum in praeparatione anti-inflammatory medicamentis, antihistamines, antifungal agentibus et aliis medicinalibus componit.
    AGROCHEMICAL Industry:Hoc compositis adhibetur in synthesim pesticides, herbicides et fungicides. Potest incorporatur in formulationibus ad augendae efficaciam contra pestes et morbos in segetes.
    Dyes et Pigmenta:II-amino-V, methylpyridine est usus, sicut praecursor pro productio morae et pigmentis. Potest converti in variis colorants in textilia, inks, pingit et coatings.
    PhotoinitiatiTors:Hoc compositis potest adhiberi ut photoinitiator in synthesim of UV-curabiles coatings, adhesives, et printing inks. Photoinitiatrors initium crosslinking profectae super nuditate ad UV lux.
    Polymer Chemistry:II-amino-V, methylpyridine adhibetur ut monomer et crosslinker in synthesis Polymeric materiae. Potest esse utilitas ad introducendam desideravit functionalities vel amplio mechanica et scelerisque proprietatibus ex polymers.
    Coordination Chymicis:Hoc compositis acts ut a versatile Ligand in coordinatione chemica et potest formare complexorum cum variis transitus metallum ions. Haec complexibus invenies uti in catalysts, sensoriis et aliis applications.
    Suus 'essential ut note quod haec applications sunt repraesentativa, et compositis potest habere additional usus, quae sunt propria quaedam industries vel investigationis areas. Semper consuleret salus data laminas sequi propriis pertractatio protocols cum operantes II-amino-V, methylpyridine.


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