About This Item
Fórmula empírica (Notação de Hill):
C14H9Cl
Número CAS:
Peso molecular:
212.67
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
95%
forma
solid
pf
77-80 °C (lit.)
densidade
1.171 g/mL at 25 °C (lit.)
grupo funcional
chloro
cadeia de caracteres SMILES
Clc1cccc2cc3ccccc3cc12
InChI
1S/C14H9Cl/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-9H
chave InChI
SRIHSAFSOOUEGL-UHFFFAOYSA-N
Descrição geral
1-Chloroanthracene forms photodimer trans-bi(1-chloro-9,10-dihydro-9,10-anthracenediyl) via the solid-state [4+4]-photodimerization.
Aplicação
1-Chloroanthracene was used to investigate the effect of polycyclic aromatic hydrocarbons on gap junctional intercellular communication and activation of intracellular receptor kinase in F344 rat liver epithelial cells.
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)
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A M Rummel et al.
Toxicological sciences : an official journal of the Society of Toxicology, 49(2), 232-240 (1999-07-23)
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Acta crystallographica. Section C, Crystal structure communications, 60(Pt 2), o146-o148 (2004-02-10)
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Since the finding in the 1930s, a large number of polycyclic aromatic hydrocarbons (PAHs) of different structures have been tested for potential tumorigenicity. Structure-activity relationships of halo-PAHs have been investigated to determine the regions of a PAH that may be
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