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II-methoxynaphthalene; Cas No.: 93-04-9

Short description:

  • Chemical nomen:II-methoxynaphthalene
  • CAS non.:93-04-9
  • Molecular formula:C11h10o
  • Molecular pondus:158.2
  • HS Code.:2909,30
  • Europae Community (EC) Number:202-213-6
  • NSC numero:(IV) CLXXI
  • UNII:Vx2t1z50c4
  • Dsstox substantia ID:DTXSID7044392
  • Nikkaji Number:J4.667a
  • Wikipedia:Β-naphthol Methyl aether
  • Wikidata:Q2240068
  • Metabolomics Workbench ID:(XLV) DCCLVIII
  • Chembl ID:Chembl195857
  • Mol file:93-04-9.mol

Product Detail

Product Tags

II-methoxynaphthalene 93-04-9

Synonyma: II-methoxynaphthalene

Chemical proprietas II-methoxynaphthalene

● species / color: alba pulveris
● Vapor Press: 0.000228MMMMMMMHG ad XXV ° C
● Melting Point: 70-73 ° C (Lit.)
● Refractive Index: 1.5440 (estimate)
● ferveret Point: CCLXXII ° C ad DCCLX Mmhg
● PKA: 0 [In XX ℃]
● Flash Point: 102.3 ° C
● Psa:9.23000
● Density: 1.072 G / CM3
● Listp: 2.84840

● Storage Taytel Taytle infra + XXX C.
● Solubility.:h2o: solutum (omnino)
● aqua Solubility.:Ensolble
● Xlogp3: 3.5
● hydrogenii vinculum donator comitem: 0
● Hydrogenii vinculum acceptor comitem: I
● Rotatable vinculum comitem: I
● Missa: 158.073164938
● Gravis Atom comitem: XII
● Complexity: CXLIV

Notitia safty

● Picogram (s):
● Codes aleam:
● Salutis statements: 22-24 / XXV

Utilis

Euge classes:Alii Classes -> Naphthalenes
Canonica ridet:CAC1 = CC2 cc = c2c = C1 =
Descriptionβ-Naphthyl METHYL Aether habet intense dulcis, flore odor suggerentes aureus flores. Est liber ex Naphthol per-odor. Dulce habet, saporem fragum. Hoc potest esse paratus a kalium β-Naphthol et methyl chloride ad CCC ° C; Per methylation β-naphthol cum Dimethyl sulfate vel per directum estterterificatio cum Methyl arcu.
Usus:II-methoxynaphthalene est immunditia non-steroidal anti-inflammatory Naproxen (N377525). II-methoxynaphthalene acylation adhibetur ut a exemplar reactionem ad studere in catalytic beneficia de Delination. Hoc quoque solebat studere alkali-metallum-mediata manganation (ammn) profectae. II-methoxynaphthalene acylation erat usus est exemplar reactionem ad studere in catalytic beneficia de Delination. Hoc quoque solebat studere alkali-metallum-mediata manganation (ammn) profectae.

Detailed introductio

II-methoxynaphthaleneNumquid a chemical compositis ex Naphalene per repositoque unum hydrogenium atom cum a Mthoxy (-och3) coetus ad locum II de Naphthalene anulum. Molecular formula est c11h10o et habet molecular pondus 158.20 P. per moleculares-methoxynaphthalene est solidum ad locus temperatus, typice apparere ut colonus in pallide crystallis. Is est a parte liquescens de 48-50 ° C.This compositis communiter usus est ut a incipiens materia in eget synthesis et organicum profectae. Est etiam assuetudo ut odor etiam in variis products, sicut unguenta et solaria, debitum ad suavis odor.

Applicatio

Sunt plures applications de II-methoxynaphthalene in variis industries. Hic paucis exempla
Fragrantia et unguentum industria:II-methoxynaphthalene est communiter ut odorem ingredient in unguibus, Colognes, et aliis odorem products. Is providet dulcis, floralis odor et saepe usus est in floralibus et orientalibus unguentis.
Silavoring Industry:Ob sua iucundum floralibus odor, II-methoxynaphthalene adhibetur ut a condignoring agente in cibum et potum industria. Potest addere floralibus vel fruity nota ad certum cibum et potum products.
Pharmaceuticals:II-methoxynaphthalene est usus in pharmaceutical investigationis et progressionem. Potest esse quod medium vel praecursor in synthesim variis pharmaceutical componit.
Chemical synthesis:Hoc compositis potest servire ut a incipiens materia vel medium in synthesis aliorum organicum componit. Est usus est in productione dyes, pigmenta, agrochemicals et specialty oeconomiae.
Research and Development:II-methoxynaphthalene communiter in officinarum investigationis et progressionem ut solvendo aut Reagent in organicum elit reactiones.
Est momenti ad note quod supra applications sunt iustus pauci exempla et non potest esse alia usus II-methoxynaphthalene in specifica industrialis vel investigationis occasus.


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