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32008

Sigma-Aldrich

1,2-Diethylbenzene

≥99.0% (GC)

Sinônimo(s):

o-Diethylbenzene

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About This Item

Fórmula linear:
C6H4(C2H5)2
Número CAS:
135-01-3
Peso molecular:
134.22
Beilstein:
1904392
Número CE:
205-170-1
Número MDL:
MFCD00009258
Código UNSPSC:
12352100
ID de substância PubChem:
57648652
NACRES:
NA.22

Ensaio

≥99.0% (GC)

temperatura de autoignição

743 °F

índice de refração

n20/D 1.502 (lit.)
n20/D 1.503

pb

183 °C (lit.)

pf

−31 °C (lit.)

densidade

0.88 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCc1ccccc1CC

InChI

1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3

chave InChI

KVNYFPKFSJIPBJ-UHFFFAOYSA-N

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Descrição geral

1,2-Diethylbenzene can be used as a reactant in the preparation of pseudocyclic diaryliodonium triflates, 5,6-disubstituted indanone intermediates via intramolecular Friedel-Crafts alkylation, dibromide intermediates via radical bromination, and in the dehydrogenative C-H/C-H arylation of indolines.

Aplicação

  • Attraction of adult Harmonia axyridis to volatiles of the insectary plant Cnidium monnieri: This study investigates the attraction of the beetle Harmonia axyridis to 1,2-diethylbenzene, indicating potential uses in biological control strategies (Zhiping et al., 2020).

Pictogramas

Flame
GHS02

Palavra indicadora

Warning

Frases de perigo

H226

Declarações de precaução

P210 - P370 + P378

Classificações de perigo

Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

131.0 °F - closed cup

Ponto de fulgor (°C)

55 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

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Formation of 4, 5, 6, 7-tetrahydroisoindoles by palladium-catalyzed hydride reduction
Hou D, et al.
The Journal of Organic Chemistry, 72 (2007)
Synthesis of arylbenziodoxoles using pseudocyclic benziodoxole triflate and arenes
Yoshimura A, et al.
ARKIVOC (Gainesville, FL, United States), 2020 (2021)
Jean-Paul Payan et al.
Archives of toxicology, 82(9), 591-600 (2008-02-07)
The bio-distribution of the neurotoxic 1,2-diethylbenzene (1,2-DEB) was studied in male Sprague-Dawley rats after intravenous administration of [(14)C] 1,2-DEB (1 mg kg(-1)). The highest concentrations of [(14)C] non-volatile metabolites, determined by whole-body auto-radiography, were in the nasal cavity, ethmoid turbinates
A M Saillenfait et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 37(11), 1089-1096 (1999-11-24)
Sprague-Dawley rats were administered 1,2-diethylbenzene (1,2-DEB) by gavage on gestational days (GD) 6 through 20 at dose levels of 0 (corn oil), 5, 15, 25 or 35 mg/kg. The dams were euthanized on GD21 and the offspring were weighed and
J P Payan et al.
Drug metabolism and disposition: the biological fate of chemicals, 29(6), 868-876 (2001-05-17)
In a previous study, it was shown that the neurotoxic compound 1,2-diethylbenzene (1,2-DEB) is mainly hydroxylated in the alkyl chain to give 1-(2'-ethylphenyl)ethanol (1,2-EPE) and excreted in urine of rats as two glucuronide compounds (GA1 and GA2). Some findings have
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