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Ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate

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Identification
Molecular formula
C13H15NO3
CAS number
10545-58-9
IUPAC name
ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate
State
State

At room temperature, ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate is typically in a solid state, most often appearing as a crystalline powder.

Melting point (Celsius)
1.00
Melting point (Kelvin)
274.15
Boiling point (Celsius)
409.00
Boiling point (Kelvin)
682.15
General information
Molecular weight
219.25g/mol
Molar mass
219.2470g/mol
Density
1.2500g/cm3
Appearence

Ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate is typically a crystalline solid that appears as a white to off-white powder. It may have a slight odor characteristic of esters.

Comment on solubility

Solubility Characteristics of Ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate

Understanding the solubility of ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate is paramount for its potential applications in organic chemistry and pharmaceuticals. The solubility of this compound can be influenced by various factors, including:

  • Polarity: Due to the presence of both hydrophobic and hydrophilic groups within its structure, this compound exhibits moderate polarity. Therefore, it is expected to possess variable solubility in different solvents.
  • Solvent Type: Ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate is likely more soluble in organic solvents such as ethanol, ethyl acetate, or dichloromethane compared to water, which might suggest limited aqueous solubility.
  • Temperature Effects: Similar to other organic compounds, the solubility of this compound may increase with temperature, allowing for better dissolution in solvent systems at higher temperatures.

To summarize, solubility is a multifaceted property that relies on a compound's structure and external conditions. Exploring the solubility of ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate not only enhances our understanding of its chemical behavior but also directs its practical applications in various fields.

Interesting facts

Interesting Facts about Ethyl 3-Methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate

Ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate is a fascinating compound known for its diverse range of applications and intriguing structural features. Here are some interesting points about this chemical:

  • Structural Uniqueness: This compound contains a complex indole structure which is notable for its varied substitution patterns. The indole ring system is ubiquitous in nature and forms the backbone of many biologically active molecules.
  • Biological Significance: Compounds with similar structures have been studied for their potential therapeutic effects. This includes properties such as antidepressant, antimicrobial, and anti-cancer activity, making tetramethylindole derivatives quite significant in medicinal chemistry.
  • Synthetic Applications: The synthesis of ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate often involves innovative organic reaction mechanisms. Researchers are continually exploring more efficient methods for its production, contributing to the development of synthetic methodologies.
  • Versatile Reactions: This compound can be incorporated into various chemical reactions, such as Condensation, Reduction, and Alkylation. These reactions allow chemists to create a wide array of derivatives, expanding the applications of this compound in different fields.
  • Impact on Research: The study of such compounds has implications beyond chemistry; it impacts fields such as biology, pharmacology, and material science. The interactions and behaviors of similar compounds have inspired countless research initiatives aimed at drug discovery and development.

In summary, ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate stands out for its structural complexity and the wide-ranging possibilities it presents. Its contributions to research reflect the ever-evolving nature of chemistry and its profound influence on various scientific disciplines.

Synonyms
7272-58-4
ethyl 3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate
BRN 0477542
4,5,6,7-Tetrahydro-3-methyl-4-oxo-indole-2-carboxylic acid ethyl ester
INDOLE-2-CARBOXYLIC ACID, 4,5,6,7-TETRAHYDRO-3-METHYL-4-OXO-, ETHYL ESTER
DTXSID90223024
5-22-06-00213 (Beilstein Handbook Reference)
DTXCID90145515
819-467-4
3-METHYL-4-OXO-4,5,6,7-TETRAHYDRO-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER
ethyl 3-methyl-4-oxo-1,5,6,7-tetrahydroindole-2-carboxylate
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester
Oprea1_794518
F1754-0022
SCHEMBL7052350
HMS1719F13
HAA27258
STK246715
AKOS000118581
SB38474
WAY-636030
NCGC00229745-01
NCGC00229745-02
DB-074608
CS-0222081
EN300-11026
VU0421338-2
G23011
AB01321707-02
AH-262/32928008
SR-01000454975
SR-01000454975-1
ethyl 3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-indole
Z57032538
2-carbethoxy-3-methyl-4-keto-4,5,6,7-tetrahydroindole
ethyl3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate