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A83008

Sigma-Aldrich

3,4-Dimethoxyaniline

98%

Synonym(s):

4-Aminopyrocatechol dimethyl ether, 4-Aminoveratrole

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About This Item

Linear Formula:
H2NC6H3(OCH3)2
CAS Number:
6315-89-5
Molecular Weight:
153.18
Beilstein/REAXYS Number:
743399
EC Number:
228-647-6
MDL number:
MFCD00008394
UNSPSC Code:
12352100
PubChem Substance ID:
24891330
NACRES:
NA.22

assay

98%

form

powder

bp

174-176 °C/22 mmHg (lit.)

mp

85-89 °C (lit.)

SMILES string

COc1ccc(N)cc1OC

InChI

1S/C8H11NO2/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5H,9H2,1-2H3

InChI key

LGDHZCLREKIGKJ-UHFFFAOYSA-N

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GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Daniela Iguchi et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 15(1), 105-116 (2015-12-24)
Photochemical reactions tend to give more than one photoproduct. However, such a reaction can be a powerful synthetic tool when it is possible to conduct it in regioselective conditions yielding a single photoproduct. Water-surfactant solutions as reaction media can be
Takashi Ikawa et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(19), 4320-4332 (2020-01-03)
Benzynes were selectively generated in situ from phenols and trapped regioselectively with potassium hexamethyldisilazide to form primary anilines following acidic workup. The direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the
Chad D Iverson et al.
Journal of chromatography. A, 1422, 186-193 (2015-10-28)
Porous graphitic carbon (PGC) is an increasingly popular and attractive phase for HPLC on account of its chemical and thermal stability, and its unique separation mechanism. However, native PGC is strongly hydrophobic and in some instances excessively retentive. As part

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