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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:
Reactant for:
- 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 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
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Direct evidence on the mechanism of the oxidation of 2, 3-dimethylindole by inorganic peroxo anions.
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ISRN Spectroscopy, 2012 (2012)
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