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T68209

Sigma-Aldrich

3,4,5-Trimethoxyaniline

97%

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About This Item

Linear Formula:
(CH3O)3C6H2NH2
CAS Number:
24313-88-0
Molecular Weight:
183.20
Beilstein/REAXYS Number:
642919
EC Number:
246-154-4
MDL number:
MFCD00008393
UNSPSC Code:
12352100
PubChem Substance ID:
24900408
NACRES:
NA.22

assay

97%

mp

110-113 °C (lit.)

SMILES string

COc1cc(N)cc(OC)c1OC

InChI

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

InChI key

XEFRNCLPPFDWAC-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H335

Hazard Classifications

Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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