140155
1,2-Dimethoxybenzene
ReagentPlus®, 99%
Synonym(s):
Pyrocatechol dimethyl ether, Veratrole
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About This Item
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Quality Level
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.)
SMILES string
COc1ccccc1OC
InChI
1S/C8H10O2/c1-9-7-5-3-4-6-8(7)10-2/h3-6H,1-2H3
InChI key
ABDKAPXRBAPSQN-UHFFFAOYSA-N
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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.
Application
1,2-Dimethoxybenzene was used to investigate the electroantennogram response of vine weevil, Otiorhynchus sulcatus to plant volatiles.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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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
Olfactory antennal responses of the vine weevil Otiorhynchus sulcatus to plant volatiles.
Entomologia Experimentalis et Applicata, 102(1), 49-64 (2002)
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
Journal of insect physiology, 49(12), 1125-1133 (2003-11-20)
Mature gregarious male desert locusts, Schistocerca gregaria, emit the courtship inhibition pheromone phenylacetonitrile. Wings and legs, in particular the fore wings, have been identified as the main releasing sites. Abdomen and head emit only trace amounts of this pheromone. In
Organic letters, 11(11), 2253-2256 (2009-05-29)
Definitive X-ray crystallographic evidence is obtained for a single hole (or a polaron) to be uniformly distributed on the three equivalent 1,2-dimethoxybenzenoid (or veratrole) rings in the hexamethoxytriptycene cation radical. This conclusion is further supported by electrochemical analysis and by
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