A83008
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:
Molecular Weight:
153.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-647-6
Beilstein/REAXYS Number:
743399
MDL number:
Product Name
3,4-Dimethoxyaniline, 98%
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
SMILES string
COc1ccc(N)cc1OC
assay
98%
form
powder
bp
174-176 °C/22 mmHg (lit.)
mp
85-89 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>230.0 °F
flash_point_c
> 110 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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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
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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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