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187712

Sigma-Aldrich

1-Chloroanthracene

95%

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About This Item

Formule empirique (notation de Hill):
C14H9Cl
Numéro CAS:
4985-70-0
Poids moléculaire :
212.67
Numéro CE :
225-641-5
Numéro MDL:
MFCD00003578
Code UNSPSC :
12352100
ID de substance PubChem :
24851284
Nomenclature NACRES :
NA.22

Pureté

95%

Forme

solid

Pf

77-80 °C (lit.)

Densité

1.171 g/mL at 25 °C (lit.)

Groupe fonctionnel

chloro

Chaîne 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

Clé InChI

SRIHSAFSOOUEGL-UHFFFAOYSA-N

Description générale

1-Chloroanthracene forms photodimer trans-bi(1-chloro-9,10-dihydro-9,10-anthracenediyl) via the solid-state [4+4]-photodimerization.

Application

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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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)
Many polycyclic aromatic hydrocarbons (PAHs) are known carcinogens. A considerable amount of research has been devoted to predicting the genotoxic, tumor-initiating potential of PAHs based on chemical structure. However, information on the correlation of structure with the non-genetoxic, epigenetic events
Ilona Turowska-Tyrk et al.
Acta crystallographica. Section C, Crystal structure communications, 60(Pt 2), o146-o148 (2004-02-10)
Crystals of the 1-chloroanthracene photodimer, viz. trans-bi(1-chloro-9,10-dihydro-9,10-anthracenediyl), C(28)H(18)Cl(2), were obtained from the solid-state [4+4]-photodimerization of the monomer, C(14)H(9)Cl, followed by recrystallization. The symmetry of the product molecules is defined by the orientation of the reactant molecules in the crystal. The
Miki Sato et al.
The Analyst, 142(23), 4560-4569 (2017-11-09)
The detection limits and photoionization thresholds of polycyclic aromatic hydrocarbons and their chlorides and nitrides on the water surface are examined using laser two-photon ionization and single-photon ionization, respectively. The laser two-photon ionization methods are highly surface-selective, with a high
Diógenes Herreno-Sáenz et al.
International journal of environmental research and public health, 3(2), 191-195 (2006-07-11)
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
Rong Jin et al.
Journal of chromatography. A, 1509, 114-122 (2017-06-18)
Isotopic dilution gas chromatography combined with high resolution mass spectrometry (GC/HRMS) has overwhelming advantages with respect to the accuracy of congener-specific ultratrace analysis of complex persistent organic pollutants (POPs) in environmental matrices. However, an isotopic dilution GC/HRMS method for analysis

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