2,6-Diphenylphenol
Names
[ CAS No. ]:
2432-11-3
[ Name ]:
2,6-Diphenylphenol
[Synonym ]:
m-Terphenyl-2'-ol
1,1':3',1''-Terphenyl-2'-ol
2,6-Ph2C6H3OH
EINECS 219-401-9
2,6-Diphenylphenol
2,5-DIMETHYL-2,5-BIS-(BENZOYLPEROXY)-HEXANE
[1,1':3',1''-Terphenyl]-2'-ol
[m-Terphenyl]-2'-ol
QR BR& FR
2'-hydroxy[1,1':3',1"]terphenyl
MFCD00009716
2'-Hydroxy-m-terphenyl
2,6-diphenyl-phenol
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
384.8±11.0 °C at 760 mmHg
[ Melting Point ]:
101-103 °C(lit.)
[ Molecular Formula ]:
C18H14O
[ Molecular Weight ]:
246.303
[ Flash Point ]:
183.2±11.1 °C
[ Exact Mass ]:
246.104462
[ PSA ]:
20.23000
[ LogP ]:
4.68
[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C
[ Index of Refraction ]:
1.626
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
Dalton Trans. 43(43) , 16197-206, (2014)
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...
Synthesis of group 1 metal 2,6-diphenylphenoxide complexes [M(OC6H3Ph2-2,6)] (M = Li, Na, K, Rb, Cs) and structures of the solvent-free complexes [Rb(OC6H3Ph2-2,6)]x and [Cs(OC6H3Ph2-2,6)x: one-dimensional extended arrays of metal aryloxides.Inorg. Chem. 42(19) , 6089-94, (2003)
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...
Clathrate formation from octaazaphthalocyanines possessing bulky phenoxyl substituents: a new cubic crystal containing solvent-filled, nanoscale voids.Chemistry 14(16) , 4810-5, (2008)
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 cav...