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Merck

120812

Sigma-Aldrich

2,3-Dimethylindole

≥97%

Sinónimos:

NSC 24936

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About This Item

Fórmula empírica (notación de Hill):
C10H11N
Número de CAS:
Peso molecular:
145.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥97%

form

solid

bp

285 °C (lit.)

mp

105-107 °C (lit.)

SMILES string

Cc1[nH]c2ccccc2c1C

InChI

1S/C10H11N/c1-7-8(2)11-10-6-4-3-5-9(7)10/h3-6,11H,1-2H3

InChI key

PYFVEIDRTLBMHG-UHFFFAOYSA-N

Application

2,3-Dimethylindole has been used to study the mechanism of oxidation of 2,3-dimethylindole by peroxodisulphate and peroxomonosulphate anions to 2-methylindole-2-carbaldehyde. It has been used to study the behaviour of methylindoles in the agilent multimode ion source by atmospheric pressure chemical ionization mass spectrometry.
Reactant for preparation of:
  • Bis(indolyl)methane derivatives
  • Potent opioid receptor agonists
  • Photorefractive materials
  • Prodrugs of the cyclin-dependent kinase (CDK) inhibitor Alsterpaullone
  • Dopamine receptors 2/4 (D2/D4) antagonists
  • Useful azaspirocyclic building blocks

Reactant for:
  • Baylis-Hillman reactions
  • Photosensitized Diels-Alder reactions
  • Photoinduced electron transfer reactions

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Direct evidence on the mechanism of the oxidation of 2, 3-dimethylindole by inorganic peroxo anions.
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Formation of the Ions of Methylindoles in APCI Mass Spectrometry.
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