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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:
642919
EC Number:
246-154-4
MDL number:
MFCD00008393
UNSPSC Code:
12352100
PubChem Substance ID:
24900408
NACRES:
NA.22

Quality Level

100

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

Signal Word

Warning

Hazard Statements

H315,H335

Hazard Classifications

Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2421
STBL2217
S42993
10626LH
S07898

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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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