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Merck
CN

T68209

3,4,5-Trimethoxyaniline

97%

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About This Item

Linear Formula:
(CH3O)3C6H2NH2
CAS Number:
Molecular Weight:
183.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-154-4
Beilstein/REAXYS Number:
642919
MDL number:
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Product Name

3,4,5-Trimethoxyaniline, 97%

InChI key

XEFRNCLPPFDWAC-UHFFFAOYSA-N

InChI

1S/C9H13NO3/c1-11-7-4-6(10)5-8(12-2)9(7)13-3/h4-5H,10H2,1-3H3

SMILES string

COc1cc(N)cc(OC)c1OC

assay

97%

mp

110-113 °C (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Romeo Romagnoli et al.
Bioorganic chemistry, 97, 103665-103665 (2020-02-23)
A new class of inhibitors of tubulin polymerization based on the 2-alkoxycarbonyl-3-(3',4',5'-trimethoxyanilino)indole molecular skeleton was synthesized and evaluated for antiproliferative activity, inhibition of tubulin polymerization and cell cycle effects. The results presented show that the methoxy substitution and location on
Gina Ambrosio et al.
Scientific reports, 10(1), 4114-4114 (2020-03-07)
Chemical reaction with diazonium molecules has revealed to be a powerful method for the surface chemical modification of graphite, carbon nanotubes and recently also of graphene. Graphene electronic structure modification using diazonium molecules is strongly influenced by graphene growth and

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