32008
1,2-Diethylbenzene
≥99.0% (GC)
Synonym(s):
o-Diethylbenzene
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About This Item
Linear Formula:
C6H4(C2H5)2
CAS Number:
Molecular Weight:
134.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-170-1
Beilstein/REAXYS Number:
1904392
MDL number:
Assay:
≥99.0% (GC)
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
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).
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signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
flash_point_f
131.0 °F - closed cup
flash_point_c
55 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 32008-1ML | 04061826695517 |
| 32008-5ML | 04061826695531 |