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A55500

Sigma-Aldrich

2-Aminofluorene

98%

Synonym(s):

2-Fluorenamine, 2-Fluorenylamine

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About This Item

Empirical Formula (Hill Notation):
C13H11N
CAS Number:
153-78-6
Molecular Weight:
181.23
Beilstein:
1945861
EC Number:
205-817-8
MDL number:
MFCD00001125
UNSPSC Code:
12352100
PubChem Substance ID:
24890992
NACRES:
NA.22

Quality Level

100

Assay

98%

form

powder

mp

124-128 °C (lit.)

SMILES string

Nc1ccc-2c(Cc3ccccc-23)c1

InChI

1S/C13H11N/c14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7,14H2

InChI key

CFRFHWQYWJMEJN-UHFFFAOYSA-N

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Related Categories

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H351,H411

Hazard Classifications

Aquatic Chronic 2 - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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In this paper, the results on horseradish peroxidase (HRP)-catalyzed oxidative polymerization of amine-functionalized fluorene monomer, 2-amino fluorene (AF), are reported. The resulting polymer exhibits an exciting molecular structure and spectral properties. FT-IR and NMR studies show that the two fluorene
Olga Rechkoblit et al.
Nature structural & molecular biology, 17(3), 379-388 (2010-02-16)
The aromatic amine carcinogen 2-aminofluorene (AF) forms covalent adducts with DNA, predominantly with guanine at the C8 position. Such lesions are bypassed by Y-family polymerases such as Dpo4 via error-free and error-prone mechanisms. We show that Dpo4 catalyzes elongation from
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