140155
1,2-Dimethoxybenzene
ReagentPlus®, 99%
Synonym(s):
Pyrocatechol dimethyl ether, Veratrole
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About This Item
Linear Formula:
C6H4(OCH3)2
CAS Number:
Molecular Weight:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-045-3
Beilstein/REAXYS Number:
1364621
MDL number:
Product Name
1,2-Dimethoxybenzene, ReagentPlus®, 99%
InChI key
ABDKAPXRBAPSQN-UHFFFAOYSA-N
InChI
1S/C8H10O2/c1-9-7-5-3-4-6-8(7)10-2/h3-6H,1-2H3
SMILES string
COc1ccccc1OC
product line
ReagentPlus®
assay
99%
refractive index
n20/D 1.533 (lit.)
bp
206-207 °C (lit.)
mp
15 °C (lit.)
solubility
alcohol: soluble
diethyl ether: soluble
fatty oils: soluble
water: slightly soluble
density
1.084 g/mL at 25 °C (lit.)
Quality Level
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Application
1,2-Dimethoxybenzene was used to investigate the electroantennogram response of vine weevil, Otiorhynchus sulcatus to plant volatiles.
General description
1,2-Dimethoxybenzene reacts with Li{N(SO2CF3)2} to yield molecular crystal [Li{N(SO2CF3)2}{C6H4(OCH3)2}2] having solid-state lithium ion conductivity. It is a potential pollinator attractant of the nocturnal moth Hadena bicruris.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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Tariq A Akhtar et al.
Plant physiology, 162(1), 52-62 (2013-04-03)
White campion (Silene latifolia) is a dioecious plant that emits 1,2-dimethoxybenzene (veratrole), a potent pollinator attractant to the nocturnal moth Hadena bicruris. Little is known about veratrole biosynthesis, although methylation of 2-methoxyphenol (guaiacol), another volatile emitted from white campion flowers
Makoto Moriya et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(40), 13554-13560 (2013-08-14)
The molecular crystals [Li{N(SO2CF3)2}{C6H4(OCH3)2}2] and [Li{N(SO2CF3)2}{C6F2H2(OCH3)2}2] with solid-state lithium ion conductivity have been synthesized by the addition of two equivalents of 1,2-dimethoxybenzene or 1,2-difluoro-4,5-dimethoxybenzene to Li{N(SO2CF3)2}, respectively. Single-crystal X-ray diffraction analysis revealed the formation of ionic conduction paths with an
Y Azuma et al.
Journal of dental research, 65(1), 53-56 (1986-01-01)
The mechanism of the anti-inflammatory action of phenolic compounds was examined using neutrophil chemotaxis. Chemotactic activity of guinea pig peritoneal neutrophils to N-formylmethionyl-leucylphenylalanine (FMLP) was suppressed in a concentration-dependent manner. The order of drug potency in inhibiting the neutrophil chemotaxis
Umma Salma Jhumur et al.
Journal of medical entomology, 43(6), 1164-1170 (2006-12-14)
Flower odors are important signals for chemical communication between plants and flower visitors. Here, we studied the naive responses of Culex pipiens pipiens biotype molestus Forskal 1775 (Diptera: Culicidae) to typical flower odors and assessed the learning capacity of mosquitoes
Yoshiya Inokuchi et al.
Physical chemistry chemical physics : PCCP, 14(13), 4457-4462 (2012-02-23)
We report UV photodissociation (UVPD) and IR-UV double-resonance spectra of 1,2-dimethoxybenzene (DMB) complexes with alkali metal ions, M(+)·DMB (M = Li, Na, K, Rb, and Cs), in a cold, 22-pole ion trap. The UVPD spectrum of the Li(+) complex shows
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