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Merck
CN

437921

4,4′-(9-Fluorenylidene)bis(2-phenoxyethanol)

97%

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About This Item

Empirical Formula (Hill Notation):
C29H26O4
CAS Number:
Molecular Weight:
438.51
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Assay:
97%
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InChI

1S/C29H26O4/c30-17-19-32-23-13-9-21(10-14-23)29(22-11-15-24(16-12-22)33-20-18-31)27-7-3-1-5-25(27)26-6-2-4-8-28(26)29/h1-16,30-31H,17-20H2

SMILES string

OCCOc1ccc(cc1)C3(c2ccc(OCCO)cc2)c4ccccc4-c5ccccc35

InChI key

NQXNYVAALXGLQT-UHFFFAOYSA-N

assay

97%

mp

117-120 °C (lit.)

General description

4,4′-(9-Fluorenylidene)bis(2-phenoxyethanol) is an aryldiol.

Application

4,4′-(9-Fluorenylidene)bis(2-phenoxyethanol) may be used for the following syntheses:
  • poly-(carbotetramethyldisiloxane)s, containing poly[oxy{4,4′-(9-fluorenylidene)bis(2-phenoxyethylene)}oxytetramethyldisiloxane] (a fluorescent aromatic chromophore group)
  • poly[oxy(arylene)oxy(tetramethyldisilylene)]s, containing fluorescent aromatic chromophore groups in the polymer main chain, via melt copolymerization reaction with 1,2-bis(diethylamino)tetramethyldisilane

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Synthesis and Properties of Poly [oxy (arylene) oxy (tetramethyldisilylene)] s via Melt Copolymerization Reaction.
Jung EA and Park YT.
Bull. Korean Chem. Soc., 34(6), 1637-1642 (2013)
Melt Copolymerization Reactions between 1, 3-Bis (diethylamino) tetramethyldisiloxane and Aryldiol Derivatives.
Jung IK and Park YT.
Bull. Korean Chem. Soc., 32(4), 1303-1309 (2011)

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