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140155

Sigma-Aldrich

1,2-Dimethoxybenzene

ReagentPlus®, 99%

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Synonym(s):
Pyrocatechol dimethyl ether, Veratrole
Linear Formula:
C6H4(OCH3)2
CAS Number:
91-16-7
Molecular Weight:
138.16
Beilstein:
1364621
EC Number:
202-045-3
MDL number:
MFCD00008357
UNSPSC Code:
12352100
PubChem Substance ID:
24848455
NACRES:
NA.22

Quality Level

100

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
Olfactory antennal responses of the vine weevil Otiorhynchus sulcatus to plant volatiles.
Tol RWHM and Visser JH.
Entomologia Experimentalis et Applicata, 102(1), 49-64 (2002)
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
Karsten Seidelmann et al.
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
Vincent J Chebny et al.
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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