Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos

152765

Sigma-Aldrich

9-Anthracenecarbonitrile

97%

Sinônimo(s):

9-Cyanoanthracene

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(1)

About This Item

Fórmula empírica (Notação de Hill):
C15H9N
Número CAS:
1210-12-4
Peso molecular:
203.24
Número CE:
214-909-7
Número MDL:
MFCD00001242
Código UNSPSC:
12352100
ID de substância PubChem:
24849258
NACRES:
NA.22

Ensaio

97%

forma

powder

pf

173-177 °C (lit.)

cadeia de caracteres SMILES

N#Cc1c2ccccc2cc3ccccc13

InChI

1S/C15H9N/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H

chave InChI

KEQZHLAEKAVZLY-UHFFFAOYSA-N

Descrição geral

The fluorescence excitation spectra of 9-anthracenecarbonitrile has been studied.

Aplicação

9-Anthracenecarbonitrile was used to study the mechanism of charge separation within phenothiazine (PTZH) or phenoxazine (PXZH), and 9-cyanoanthracene(electron acceptor).

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302 + H312 + H332

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

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

dust mask type N95 (US), Eyeshields, Gloves

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”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 7

1 of 7

9-Methylanthracene 98%

Sigma-Aldrich

M29606

9-Methylanthracene

4-Ethynylbenzonitrile 97%

Sigma-Aldrich

206539

4-Ethynylbenzonitrile

Anthracene ReagentPlus®, 99%

Sigma-Aldrich

141062

Anthracene

1,4-Dicyanobenzene 98%

Sigma-Aldrich

D76722

1,4-Dicyanobenzene

Anthracene for synthesis

Sigma-Aldrich

8.20109

Anthracene

1-Aminoanthraquinone ≥96.5% (HPLC)

Sigma-Aldrich

A39009

1-Aminoanthraquinone

2,6-Diaminoanthraquinone 97%

Sigma-Aldrich

D12007

2,6-Diaminoanthraquinone

M Takahashi et al.
Journal of pharmaceutical and biomedical analysis, 14(11), 1579-1584 (1996-08-01)
9-Anthroylnitrile was used as an achiral reagent for the derivatization of carnitine. The reagent forms UV-absorbing derivatives with the hydroxyl groups of carnitine enantiomers under very mild conditions. The derivatives were separated by high-performance liquid chromatography on an ovomucoid-conjugated column
Barbara Pliszka et al.
Biochimica et biophysica acta, 1699(1-2), 201-205 (2004-05-26)
The fluorescent probe, 9-anthroylnitrile (ANN), can selectively attach to Ser-180 at the ATP-binding site of subfragment 1 (S1) of skeletal muscle myosin [J. Biol. Chem. 278 (2003) 31891]. We have found that MgATP, MgATPgammaS, MgADP.AlF(4) or MgPP(i), but not MgADP
Toshiaki Hiratsuka et al.
The Journal of biological chemistry, 278(34), 31891-31894 (2003-06-14)
The esterification reagent 9-anthroylnitrile (ANN) reacts with a serine residue in the NH2-terminal 23-kDa peptide segment of myosin subfragment-1 heavy chain to yield a fluorescent S1 derivative labeled by the anthroyl group (Hiratsuka, T. (1989) J. Biol. Chem. 264, 18188-18194).
Misako Takahashi et al.
Journal of chromatography. A, 958(1-2), 299-303 (2002-07-24)
HPLC with fluorescence detection was used for the determination of low levels of liothyronine sodium and levothyroxine sodium in pharmaceutical preparations after fluorogenic derivatization. 9-Anthroylnitrile in dimethyl sulfoxide was used as a precolumn fluorogenic reagent. The 9-anthroylnitrile derivatives of liothyronine
T Hiratsuka
The Journal of biological chemistry, 265(31), 18786-18790 (1990-11-05)
A fluorophore, 9-anthroyl (AN) group, was covalently incorporated into the 23-kDa NH2-terminal peptide segment of myosin subfragment-1 (S-1) (Hiratsuka, T. (1989) J. Biol. Chem. 264, 18188-18194). The fluorescent S-1 derivative (AN-S-1) was utilized to detect conformational changes in the 23-kDa
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica