180637
9-Hydroxy-9-fluorenecarboxylic acid
96%
Synonym(s):
Flurenol, 9-Hydroxyfluorene-9-carboxylic acid
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All Photos(3)
About This Item
Empirical Formula (Hill Notation):
C14H10O3
CAS Number:
Molecular Weight:
226.23
Beilstein/REAXYS Number:
1314711
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
96%
mp
162-166 °C (lit.)
functional group
carboxylic acid
hydroxyl
SMILES string
OC(=O)C1(O)c2ccccc2-c3ccccc13
InChI
1S/C14H10O3/c15-13(16)14(17)11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8,17H,(H,15,16)
InChI key
GXAMYUGOODKVRM-UHFFFAOYSA-N
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Application
9-Hydroxy-9-fluorenecarboxylic acid was used in the synthesis of a hexameric organooxotin prismane.
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Vadapalli Chandrasekhar et al.
Journal of the American Chemical Society, 127(33), 11556-11557 (2005-08-18)
A hydroxyl-rich hexameric organooxotin prismane has been prepared by reaction of n-BuSn(O)OH with 9-hydroxy-9-fluorenecarboxylic acid. The supramolecular structure of this cage shows channels with hydrophobic and hydrophilic segments, which selectively entrap guest molecules.
Yusuke Nakajima et al.
Journal of experimental botany, 68(13), 3441-3456 (2017-06-22)
The direction of auxin transport changes in gravistimulated roots, causing auxin accumulation in the lower side of horizontally reoriented roots. This study found that auxin was similarly involved in hydrotropism and gravitropism in rice and pea roots, but hydrotropism in
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