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F1204

Sigma-Aldrich

Fluorene-1-carboxylic acid

97%

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About This Item

Empirical Formula (Hill Notation):
C14H10O2
CAS Number:
Molecular Weight:
210.23
Beilstein/REAXYS Number:
2330772
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

246-248 °C (lit.)

SMILES string

OC(=O)c1cccc-2c1Cc3ccccc-23

InChI

1S/C14H10O2/c15-14(16)12-7-3-6-11-10-5-2-1-4-9(10)8-13(11)12/h1-7H,8H2,(H,15,16)

InChI key

HTPXFGUCAUTOEL-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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William Kemnitzer et al.
Bioorganic & medicinal chemistry letters, 20(3), 1288-1292 (2009-12-26)
As a continuation of our studies of apoptosis inducing 9-oxo-9H-fluorene-1-carboxamides as potential anticancer agents, we explored modification of the 9-oxo-9H-fluorene ring. SAR studies showed that most changes to the 9-oxo-9H-fluorene ring were not well tolerated, except the 9H-fluorene (2b) and
A C Blackburn et al.
Acta crystallographica. Section C, Crystal structure communications, 52 ( Pt 4), 907-910 (1996-04-15)
In fluorene-1-carboxylic acid, C14H10O2, the sole hydrogen bond is of the cyclic dimer type about a center of symmetry. The carboxyl H atom is ordered. Distances in the fluorene core are very similar to those in fluorene itself; the fluorene

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