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DMNITC

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Identification
Molecular formula
C12H13N3O2
CAS number
98007-97-9
IUPAC name
N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine
State
State

At room temperature, DMNITC is a solid, typically encountered as a crystalline powder.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
246.27g/mol
Molar mass
246.2720g/mol
Density
1.2800g/cm3
Appearence

DMNITC is typically present as a crystalline solid with a yellowish hue. It may be sensitive to light, resulting in slight variations in coloration over time.

Comment on solubility

Solubility of N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine

N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine, often referred to as a heterocyclic amine derivative, presents interesting characteristics concerning its solubility in various solvents.

Solubility Factors:

  • Polarity: The presence of both amine and nitro groups contributes to the molecule’s polar characteristics, which enhances solubility in polar solvents.
  • Hydrogen Bonding: The amine group can engage in hydrogen bonding, leading to increased solubility in water.
  • Organic Solvents: This compound is likely to be soluble in a range of organic solvents due to its non-polar hydrocarbon structure associated with the indole moiety.

In general, the solubility of this compound can be summarized as follows:

  1. Highly soluble in: Polar solvents like water and methanol.
  2. Moderately soluble in: Organic solvents such as ethanol and acetone.
  3. Limited solubility in: Non-polar solvents like hexane.

Thus, understanding these solubility dynamics is crucial for applications involving N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine in both research and industrial contexts. Its solubility properties enhance its utility in chemical synthesis and pharmaceutical formulations.

Interesting facts

Interesting Facts about N,N-Dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine

N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine is a fascinating chemical compound with a variety of implications in the fields of organic chemistry, pharmacology, and materials science. Here are some intriguing aspects of this compound:

  • Structural Significance: This compound is characterized by the presence of an indole skeleton, which is a significant structure in many natural products and pharmaceuticals. Indoles are known for their diverse biological activities and are often found in drugs.
  • Pharmaceutical Relevance: The nitro group attached to the indole ring suggests potential applications in medicinal chemistry, particularly in the development of novel therapeutic agents. Nitrogen-containing compounds often exhibit interesting pharmacological properties that can enhance efficacy.
  • Synthetic Pathways: The synthesis of N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine showcases the beauty of organic reactions. Chemists utilize various synthetic routes to create such compounds, often involving the functionalization of the indole moiety.
  • Research Potential: Ongoing research is focused on exploring the biological activity of compounds that feature indole derivatives. This compound may contribute to studies in cancer research, neuropharmacology, or as a precursor in the design of new molecular probes.
  • Interdisciplinary Applications: Beyond pharmacology, the compound's properties may find utility in fields such as materials science, where its unique structure can lead to the development of novel dyes or sensors.

As researchers continue to explore the diverse applications of N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine, it is evident that the interplay of its structural features and potential biological activity makes it a compound worthy of further investigation.

Synonyms
7-Nitrogramine
1654-34-8
NSC 70813
BRN 0480620
INDOLE, 3-((DIMETHYLAMINO)METHYL)-7-NITRO-
DTXSID00167940
5-22-10-00037 (Beilstein Handbook Reference)
DTXCID8090431
N,N-dimethyl-1-(7-nitro-1H-indol-3-yl)methanamine
3-(Dimethylamino)-7-nitro-1H-indole
NSC70813
SCHEMBL260846
YLVPUBNLOINGDI-UHFFFAOYSA-N
NSC-70813
BS-27402