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Merck
CN

180637

9-Hydroxy-9-fluorenecarboxylic acid

96%

Synonym(s):

Flurenol, 9-Hydroxyfluorene-9-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C14H10O3
CAS Number:
Molecular Weight:
226.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-397-1
Beilstein/REAXYS Number:
1314711
MDL number:
Assay:
96%
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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

Application

9-Hydroxy-9-fluorenecarboxylic acid was used in the synthesis of a hexameric organooxotin prismane.


pictograms

Environment

hcodes

pcodes

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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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



Global Trade Item Number

SKUGTIN
180637-25G04061836691417