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A55500

Sigma-Aldrich

2-Aminofluorene

98%

Sinônimo(s):

2-Fluorenamine, 2-Fluorenylamine

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About This Item

Fórmula empírica (Notação de Hill):
C13H11N
Número CAS:
153-78-6
Peso molecular:
181.23
Beilstein:
1945861
Número CE:
205-817-8
Número MDL:
MFCD00001125
Código UNSPSC:
12352100
ID de substância PubChem:
24890992
NACRES:
NA.22

Nível de qualidade

100

Ensaio

98%

forma

powder

pf

124-128 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

CFRFHWQYWJMEJN-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Health hazardEnvironment
GHS08,GHS09

Palavra indicadora

Warning

Frases de perigo

H351,H411

Classificações de perigo

Aquatic Chronic 2 - Carc. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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2-Nitro-9-fluorenone 99%

Sigma-Aldrich

299758

2-Nitro-9-fluorenone

Ali Bilici et al.
Biomacromolecules, 11(10), 2593-2601 (2010-09-08)
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
Jun Zhao et al.
Stem cell research & therapy, 10(1), 165-165 (2019-06-15)
Mounting evidence has shown that a novel subset of mesenchymal stem cells (MSCs) derived from human gingiva referred to as gingival mesenchymal stem cells (GMSCs) displays a greater immunotherapeutic potential and regenerative repair expression than MSCs obtained from other tissues.
R H Heflich et al.
Mutation research, 318(2), 73-114 (1994-10-01)
2-Acetylaminofluorene and 2-aminofluorene are among the most intensively studied of all chemical mutagens and carcinogens. Fundamental research findings concerning the metabolism of 2-acetylaminofluorene to electrophilic derivatives, the interaction of these derivatives with DNA, and the carcinogenic and mutagenic responses that
Nidhi Jain et al.
Chemical research in toxicology, 21(2), 445-452 (2008-01-16)
Fluorescence spectroscopy was used to study carcinogen-induced conformational heterogeneity in DNA duplexes. The fluorophore 2-aminopurine (AP) was incorporated adjacent (5') to the lesion (G*) in eight different DNA duplexes [d(5'-CTTCT PG* NCCTC-3'):d(5'-GAGGN XTAGAAG-3'), G* = FAF adduct, P = AP
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