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2-Methylindole

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For Research Use Only | Not For Clinical Use
CATAP95205
CAS95-20-5
Structure
MDL NumberMFCD00005616
Molecular Weight131.17
EC Number202-398-3
InChI KeyBHNHHSOHWZKFOX-UHFFFAOYSA-N
REAXYS Number109781
Descriptionanalytical standard
Assay≥98.0% (HPLC)
BP273 °C (lit.)
Gradeanalytical standard
MP57-59 °C (lit.)
Size100MG
1

Dehydrogenation of the Liquid Organic Hydrogen Carrier System 2-methylindole/2-methylindoline/2-methyloctahydroindole on Pt(111)

Philipp Bachmann, Johann Steinhauer, Florian Späth, Fabian Düll, Udo Bauer, Roman Eschenbacher, Felix Hemauer, Marlene Scheuermeyer, Andreas Bösmann, Miriam Büttner, Christian Neiß, Andreas Görling, Peter Wasserscheid, etc.

J Chem Phys. 2019 Oct 14;151(14):144711.

PMID: 31615244

1

Homogeneously-catalysed Hydrogen release/storage Using the 2-methylindole/2-methylindoline LOHC System in Molten Salt-Organic Biphasic Reaction Systems

Alexander Søgaard, Marlene Scheuermeyer, Andreas Bösmann, Peter Wasserscheid, Anders Riisager

Chem Commun (Camb). 2019 Feb 12;55(14):2046-2049.

PMID: 30687857

1

Mono-methylindoles Induce CYP1A Genes and Inhibit CYP1A1 Enzyme Activity in Human Hepatocytes and HepaRG Cells

Barbora Vyhlídalová, Karolína Poulíková, Iveta Bartoňková, Kristýna Krasulová, Jan Vančo, Zdeněk Trávníček, Sridhar Mani, Zdeněk Dvořák

Toxicol Lett. 2019 Oct 1;313:66-76.

PMID: 31201936

1

Spectroscopic Study of 2-methylindole and 3-methylindole: Solvents Interactions and DFT Studies

Saheed A Popoola

Spectrochim Acta A Mol Biomol Spectrosc. 2018 Jan 15;189:578-585.

PMID: 28881283

1

Synthesis of Biologically Active 1'-(2-oxo-2H-benzopyran-6-yl)- 5'-hydroxy-2'-methylindole-3'-amido-2"-phenyl-thiazolidene-4"-ones

Vinata V Mulwad, Hitesh T Parmar, Abid A Mir

Acta Pol Pharm. Jan-Feb 2011;68(1):49-55.

PMID: 21485701

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