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
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
mp
117-120 °C (lit.)
SMILES string
OCCOc1ccc(cc1)C3(c2ccc(OCCO)cc2)c4ccccc4-c5ccccc35
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
InChI key
NQXNYVAALXGLQT-UHFFFAOYSA-N
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)[1]
- 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[2]
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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