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Merck
CN

233595

2,6-二苯基苯酚

98%

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关于此项目

线性分子式:
(C6H5)2C6H3OH
化学文摘社编号:
分子量:
246.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-401-9
MDL number:
Assay:
98%
Form:
solid
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Quality Level

assay

98%

form

solid

mp

101-103 °C (lit.)

functional group

phenyl

SMILES string

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

InChI key

ATGFTMUSEPZNJD-UHFFFAOYSA-N

General description

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.

Application

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


pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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



全球贸易项目编号

货号GTIN
233595-1G04061826279205
233595-25G04061832880013
233595-5G04061838784063