Passa al contenuto
Merck
Tutte le immagini(1)

Key Documents

Altri documenti

233595

Sigma-Aldrich

2,6-Diphenylphenol

98%

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
(C6H5)2C6H3OH
Numero CAS:
2432-11-3
Peso molecolare:
246.30
Numero CE:
219-401-9
Numero MDL:
MFCD00009716
Codice UNSPSC:
12352100
ID PubChem:
24853986
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

Punto di fusione

101-103 °C (lit.)

Stringa SMILE

Oc1c(cccc1-c2ccccc2)-c3ccccc3

InChI

1S/C18H14O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h1-13,19H
ATGFTMUSEPZNJD-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

2,6-Diphenylphenol reacts with with (n)BuLi, NaH, KH, or Rb or Cs metal in benzene to yield the solvent-free complexes [M(OAr)]x.

Applicazioni

2,6-Diphenylphenol has been used:
  • as ligand during the synthesis of reduced coordination (less than 6), unchelated manganese oxygen cluster systems
  • in the preparation of derivatives of pyrazine-2,3-dicarbonitrile, precursor required for the synthesis of octaazaphthalocyanine (AzaPc) derivatives

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 2

1 of 2

Copper(I) chloride AnhydroBeads™, ≥99.99% trace metals basis

Sigma-Aldrich

651745

Copper(I) chloride

Adsorbente polimerico poroso Tenax® matrix Tenax TA, 60-80 mesh, bottle of 10 g

Supelco

11982

Adsorbente polimerico poroso Tenax®

Saad Makhseed et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(16), 4810-4815 (2008-05-01)
The synthesis of octaazaphthalocyanine (AzaPc) derivatives, with bulky phenoxyl substituents placed at eight peripheral positions and containing either H(+), Ni(2+) or Zn(2+) ions in their central cavity, is described. The required precursors, derivatives of pyrazine-2,3-dicarbonitrile, were prepared using a nucleophilic
Charles S Weinert et al.
Inorganic chemistry, 42(19), 6089-6094 (2003-09-16)
Reaction of 2,6-diphenylphenol (HOC(6)H(3)Ph(2)-2,6) with (n)BuLi, NaH, KH, or Rb or Cs metal in benzene gives the solvent-free complexes [M(OAr)]x in excellent yield. The complex [Rb(OC(6)H(3)Ph(2)-2,6)](x)() exhibits a ladderlike structure in the solid state with triply bridging oxygen atoms and
Sandeep K Kondaveeti et al.
Inorganic chemistry, 51(19), 10095-10104 (2012-09-06)
The synthesis of reduced coordination (less than 6), unchelated manganese oxygen cluster systems is described. Addition of phenols to Mn(NR(2))(2) (R = SiMe(3)) results in protolytic amide ligand replacement, and represents the primary entry into the described chemistry. Addition of
Camilo J Viasus et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(68), 17269-17278 (2017-10-17)
The reactivity of carbon dioxide with vanadium(III) aryloxo complexes has been investigated. The formation of either carbon monoxide or incorporation into the ligand system with the ultimate formation of organic ester was observed depending on the overall electron donor ability
Ursula J Williams et al.
Dalton transactions (Cambridge, England : 2003), 43(43), 16197-16206 (2014-08-26)
The trivalent compound K[Ce[N(SiHMe2)2]4] was synthesized and oxidized, providing a convenient route to the reported cerium(IV) compound Ce[N(SiHMe2)2]4. Protonolysis reactions of Ce[N(SiHMe2)2]4 with tert-butanol, substituted benzyl alcohols, and 2,6-diphenylphenol yielded the neutral tetravalent compounds Ce(O(t)Bu)4(py)2, Ce2(OCH2C6R5)8(thf)2 (R = Me, F)

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.