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Merck
CN

160504

9-Fluorenemethanol

99%

Synonym(s):

9-(Hydroxymethyl)fluorene, 9-Fluorenylmethanol

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About This Item

Empirical Formula (Hill Notation):
C14H12O
CAS Number:
24324-17-2
Molecular Weight:
196.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849874
EC Number:
246-167-5
Beilstein/REAXYS Number:
2330017
MDL number:
MFCD00001139

Key Documents

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Product Name

9-Fluorenemethanol, 99%

InChI key

XXSCONYSQQLHTH-UHFFFAOYSA-N

InChI

1S/C14H12O/c15-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14-15H,9H2

SMILES string

OCC1c2ccccc2-c3ccccc13

assay

99%

form

solid

mp

105-107 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear (very hazy colorless to yellow and Colorless to Green-Yellow)

functional group

hydroxyl

Quality Level

200

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Application

9-Fluorenemethanol, N-protecting reagent, was used in the peptide syntheses. 9-Fluorenemethanol was also used in the synthesis of deoxynucleoside 9-fluorenemethyl phosphorodithioates.

General description

Vibrational spectroscopy of jet-cooled 9-fluorenemethanol and its clusters 9-fluorenemethanol-H2O, 9-fluorenemethanol-CH3OH, 9-fluorenemethanol-C2H5OH and 9-fluorenemethanol-C3H7OH has been studied by IR-UV double-resonance method. Electropolymerization of 9-fluorenemethanol in boron trifluoride diethyl etherate leads to low-potential electrodeposition of semiconducting poly(9-fluorenemethanol) (PFMO) film.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0001431920
1431920
0001428746
1428746V
1428747

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2'-Deoxynucleoside Dithiophosphates: Synthesis and Biological Studies1.
Seeberger PH, et al.
Journal of the American Chemical Society, 117(5), 1472-1478 (1995)
Synthesis, 119-119 (1990)
Swarna Basu et al.
The Journal of chemical physics, 120(12), 5631-5641 (2004-07-23)
Vibrational spectroscopy of jet-cooled 9-fluorenemethanol and its clusters 9-fluorenemethanol-H2O, 9-fluorenemethanol-CH3OH, 9-fluorenemethanol-C2H5OH, and 9-fluorenemethanol-C3H7OH has been carried out using an IR-UV double-resonance method. The spectrum of the OH stretching vibration, v(OH), has been measured for the 9-fluorenemethanol monomer and for each
Low-potential electrosynthesis of novel electroactive poly (9-fluorenemethanol) and its electrochromic and blue-light-emitting properties.
Zhang S, et al.
Electrochimica Acta, 90, 452-460 (2013)
The Journal of Organic Chemistry, 57, 6421-6421 (1992)
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