180637
9-Hydroxy-9-fluorenecarboxylic acid
96%
Synonym(s):
Flurenol, 9-Hydroxyfluorene-9-carboxylic acid
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5 G
£23.05
25 G
£101.00
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5 G
£23.05
25 G
£101.00
About This Item
Empirical Formula (Hill Notation):
C14H10O3
CAS Number:
Molecular Weight:
226.23
Beilstein:
1314711
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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[1].
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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