Atomfair 2,4-Dimethyl-1H-indole C10H11N CAS 10299-61-3

2,4-Dimethyl-1H-indole (CAS No. 10299-61-3) is a high-purity heterocyclic organic compound with the molecular formula C10H11N. This indole derivative is characterized by its two methyl substituents at the 2- and 4-positions of the indole ring, offering unique reactivity and structural features for advanced synthetic applications. With a molecular weight of 145.20 g/mol, this compound is a valuable building block in pharmaceutical, agrochemical, and material science research. Its crystalline solid form and stability under standard conditions ensure reliable performance in diverse experimental settings. Ideal for use as an intermediate in the synthesis of complex molecules, 2,4-Dimethyl-1H-indole is rigorously tested for purity and…

Description

2,4-Dimethyl-1H-indole (CAS No. 10299-61-3) is a high-purity heterocyclic organic compound with the molecular formula C10H11N. This indole derivative is characterized by its two methyl substituents at the 2- and 4-positions of the indole ring, offering unique reactivity and structural features for advanced synthetic applications. With a molecular weight of 145.20 g/mol, this compound is a valuable building block in pharmaceutical, agrochemical, and material science research. Its crystalline solid form and stability under standard conditions ensure reliable performance in diverse experimental settings. Ideal for use as an intermediate in the synthesis of complex molecules, 2,4-Dimethyl-1H-indole is rigorously tested for purity and consistency, making it a trusted choice for researchers and industrial chemists.

Properties

  • CAS Number: 10299-61-3
  • Complexity: 144
  • IUPAC Name: 2,4-dimethyl-1H-indole
  • InChI: InChI=1S/C10H11N/c1-7-4-3-5-10-9(7)6-8(2)11-10/h3-6,11H,1-2H3
  • InChI Key: YBUMNVFXMLIKDZ-UHFFFAOYSA-N
  • Exact Mass: 145.089149355
  • Molecular Formula: C10H11N
  • Molecular Weight: 145.20
  • SMILES: CC1=C2C=C(NC2=CC=C1)C
  • Topological: 15.8
  • Monoisotopic Mass: 145.089149355
  • Synonyms: 2,4-dimethyl-1H-indole, 2,4-dimethylindole, DTXSID70451166, DTXCID90401986, ybumnvfxmlikdz-uhfffaoysa-n, 10299-61-3, MFCD09701270, 2,4 dimethyl indole, SCHEMBL2931891, SCHEMBL6206899, SCHEMBL8230643, SCHEMBL10576531, SCHEMBL28144663, CHEBI:169202, AKOS006331463, SB30276, DB-058900, CS-0342291, C14038

Application

2,4-Dimethyl-1H-indole serves as a versatile intermediate in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals. Its structural motif is frequently employed in the development of indole-based alkaloids and receptor-targeting molecules. Researchers also utilize this compound in material science for the design of organic semiconductors and fluorescent dyes.

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