Saltar al contenido
Merck

32008

Sigma-Aldrich

1,2-Diethylbenzene

≥99.0% (GC)

Sinónimos:

o-Diethylbenzene

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
C6H4(C2H5)2
Número de CAS:
Peso molecular:
134.22
Beilstein/REAXYS Number:
1904392
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99.0% (GC)

autoignition temp.

743 °F

refractive index

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

bp

183 °C (lit.)

mp

−31 °C (lit.)

density

0.88 g/mL at 25 °C (lit.)

SMILES string

CCc1ccccc1CC

InChI

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

InChI key

KVNYFPKFSJIPBJ-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

General description

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.

Application

  • 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).

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

131.0 °F - closed cup

flash_point_c

55 °C - closed cup

ppe

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


Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Synthesis of arylbenziodoxoles using pseudocyclic benziodoxole triflate and arenes
Yoshimura A, et al.
ARKIVOC (Gainesville, FL, United States), 2020 (2021)
Formation of 4, 5, 6, 7-tetrahydroisoindoles by palladium-catalyzed hydride reduction
Hou D, et al.
The Journal of Organic Chemistry, 72 (2007)
Exceptionally Mild Palladium (II)-Catalyzed Dehydrogenative C--H/C--H Arylation of Indolines at the C-7 Position under Air
Jiao L, et al.
Organic Letters, 16 (2014)
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
I Linhart et al.
Xenobiotica; the fate of foreign compounds in biological systems, 26(12), 1263-1272 (1996-12-01)
1. Biotransformation of 1,2-diethenylbenzene (1) in rat was studied. Five urinary metabolites were isolated by extraction of acid hydrolysed urine and identified by nmr and mass spectroscopy, namely, 1-(2-ethenylphenyl)ethane-1,2-diol (2) 2-ethenylmandelic acid (3), 2-ethenylphenylglyoxylic acid (4), 2-ethenylphenylacetylglycine (5) N-acetyl-S-[1-(2-ethenylphenyl)-2-hydroxyethyl]cysteine (6)

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico