Molecular structure of 1,2-Dimethylindole, CAS Number: 875-79-6
1,2-Dimethylindole (CAS 875-79-6)
Application:
1,2-Dimethylindole is a versatile building block for organic syntheses
CAS Number:
875-79-6
Molecular Weight:
145.20
Molecular Formula:
C10H11N
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1,2-Dimethylindole is a versatile building block for the preparation of carboxyindoles, 3-functionalized indoles, cyanoindoles, carbazoles, and trifluoromethylindoles. 1,2-Dimethylindole is also used as a reagent in Nazarov cyclizations, and in the preparation of plant growth promoters, tryptophan derivatives, and antihyperlipidemic agents. 1,2-Dimethylindole is a cyclic hydrocarbon characterized by its insolubility in water, while displaying solubility in alcohol and ether.
1,2-Dimethylindole (CAS 875-79-6) References
- Gold(I)-catalyzed intramolecular enantioselective hydroarylation of allenes with indoles. | Liu, C. and Widenhoefer, RA. 2007. Org Lett. 9: 1935-8. PMID: 17428061
- Gold(I)-Catalyzed Hydroarylation of Allenes with Indoles. | Toups, KL., et al. 2009. J Organomet Chem. 694: 571-575. PMID: 20305794
- Silylated cyclopentadienes as competent silicon Lewis acid catalysts. | Radtke, MA. and Lambert, TH. 2018. Chem Sci. 9: 6406-6410. PMID: 30310569
- Annulative π-extension of indoles and pyrroles with diiodobiaryls by Pd catalysis: rapid synthesis of nitrogen-containing polycyclic aromatic compounds. | Kitano, H., et al. 2018. Chem Sci. 9: 7556-7561. PMID: 30319756
- Generation of indole derivatives by an endophytic fungus Chaetomium sp. through feeding 1,2-dimethylindole. | Jin, X., et al. 2022. Nat Prod Res. 36: 87-95. PMID: 32380913
- B(C6F5)3-Catalyzed Direct C3 Alkylation of Indoles and Oxindoles. | Basak, S., et al. 2020. ACS Catal. 10: 4835-4840. PMID: 32596025
- In Vitro Gastrointestinal Digestion Impact on the Bioaccessibility and Antioxidant Capacity of Bioactive Compounds from Tomato Flours Obtained after Conventional and Ohmic Heating Extraction. | Coelho, MC., et al. 2021. Foods. 10: PMID: 33800085
- Organophosphorus-catalyzed relay oxidation of H-Bpin: electrophilic C-H borylation of heteroarenes. | Lipshultz, JM., et al. 2020. Chem Sci. 12: 1031-1037. PMID: 34163869
- Copper catalyzed late-stage C(sp3)-H functionalization of nitrogen heterocycles. | Chang, Z., et al. 2021. Nat Commun. 12: 4342. PMID: 34267229
- Perspectives on strategies for improving ultra-deep desulfurization of liquid fuels through hydrotreatment: Catalyst improvement and feedstock pre-treatment. | Dembaremba, TO., et al. 2022. Front Chem. 10: 807225. PMID: 35936099
- One-Pot Synthesis of Styrene Derivatives from Allyl Silanes via B(C6F5)3-Catalyzed Isomerization-Hiyama Coupling. | Kustiana, BA., et al. 2022. Org Lett. 24: 8694-8697. PMID: 36394303
- Silver-catalyzed direct selanylation of indoles: synthesis and mechanistic insights. | Rios, EAM., et al. 2023. RSC Adv. 13: 914-925. PMID: 36686957
- Thermodynamic Analysis of Chemical Hydrogen Storage: Energetics of Liquid Organic Hydrogen Carrier Systems Based on Methyl-Substituted Indoles. | Vostrikov, SV., et al. 2023. Materials (Basel). 16: PMID: 37049216
- Heterogeneous Catalysts in N-Heterocycles and Aromatics as Liquid Organic Hydrogen Carriers (LOHCs): History, Present Status and Future. | Zhang, J., et al. 2023. Materials (Basel). 16: PMID: 37241361
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,2-Dimethylindole, 5 g | sc-253966 | 5 g | $116.00 |