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391573

Sigma-Aldrich

1-Bromopyrene

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Disponível para enviar em22 de abril de 2025Detalhes


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1 G
R$ 539,00

About This Item

Fórmula empírica (Notação de Hill):
C16H9Br
Número CAS:
Peso molecular:
281.15
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

R$ 539,00


Disponível para enviar em22 de abril de 2025Detalhes


Solicite uma grande encomenda

Nível de qualidade

Ensaio

96%

Formulário

powder

pf

102-105 °C (lit.)

grupo funcional

bromo

cadeia de caracteres SMILES

Brc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H9Br/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H

chave InChI

HYGLETVERPVXOS-UHFFFAOYSA-N

Descrição geral

1-Bromopyrene, a polycyclic aromatic hydrocarbon (PAH)[1], is a mono bromo substituted pyrene derivative. Its synthesis has been reported.[2] Its gas phase UV-absorption spectra in the UV wavelength range at elevated temperature has been studied.[3] Electron affinitiy (EA) of 1-bromopyrene has been investigated using electron attachment desorption chemical ionization mass spectrometry (DCI-MS) and triple quadrupole tandem mass spectrometry.[4] It participates in the synthesis of novel ruthenium (II) bipyridine or terpyridine complexes bearing pyrene moiety.[5] The reaction of 1-bromopyrene cation radical with water in acetonitrile has been analyzed using the electron transfer stopped-flow (ETSF) method.[6]

Aplicação

1-Bromopyrene is suitable reagent used in the comparative study of effect of substituents of some pyrene derivatives in inducing phototoxicity, DNA damage and repair in human skin keratinocytes[1] and light-induced lipid peroxidation in methanol.[7] It is suitable reagent used in the study to investigate the UV photon-assisted thermal decomposition of PAHs at elevated temperature.[8]
1-Bromopyrene may be used as a standard to compare its spectral properties with that of pyrene based fluorescence probe.[9] It may be used to study the effects of the addition of halogen hetero-atoms on the vapor pressures and thermodynamics of polycyclic aromatic hydrocarbons.[10]
It may be used in the synthesis of the following:
  • 2-methyl-4-pyren-1-yl-but-3-yn-2-ol[2]
  • 1-ethynylpyrene[2]
  • silsesquioxane (SSQ) based hybrid[11]
  • ruthenium nanoparticles functionalized with pyrene moiety[12]
  • mono- and di-pyrenyl perfluoroalkanes[13]
  • oligo(1-bromopyrene)(OBrP) films[14]
  • dinitropyrene-derived DNA adduct[15]

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

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


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Syntheses of mono-and di-pyrenyl perfluoroalkanes.
Wiedenfeld D, et al.
Journal of Fluorine Chemistry, 104(2), 303-306 (2000)
Gas-phase UV spectroscopy of anthracene, xanthone, pyrene, 1-bromopyrene and 1, 2, 4-trichlorobenzene at elevated temperatures.
Thony A and Rossi MJ.
Journal of Photochemistry and Photobiology A: Chemistry, 104(1), 25-33 (1997)
M Shou et al.
Drug metabolism and disposition: the biological fate of chemicals, 16(2), 173-183 (1988-03-01)
Due to the symmetrical property of pyrene (Py), trans-dihydrodiols formed at 4,5- and 9,10-positions are identical, as are the monohydroxylated products (phenols) formed at C1, C3, C6, and C8 positions. With a bromo substituent at C1 position of Py, 1-bromopyrene
Shu-Wen Yang et al.
The journal of physical chemistry. B, 109(35), 16628-16635 (2006-07-21)
An attempt to tune the electronic properties of pyrene (Py) by coupling it with a strong electron donor (-PhNMe2, DMA)/acceptor (anthronitrile, AN) through an ethynyl bridge has been undertaken. A moderate electron donor (iPrOPh-, IPP)/acceptor (2-quinolinyl, 2Q) has also been
Organic-inorganic hybrids based on pyrene functionalized octavinylsilsesquioxane cores for application in OLEDs.
Mee Yoon Lo et al.
Journal of the American Chemical Society, 129(18), 5808-5809 (2007-04-13)

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