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Troponeimine

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Identification
Molecular formula
C7H7NO
CAS number
487-91-2
IUPAC name
2-aminocyclohepta-2,4,6-trien-1-one
State
State

At room temperature, 2-aminocyclohepta-2,4,6-trien-1-one exists as a solid. It possesses a distinct aroma, a trait common to aromatic compounds.

Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
119.14g/mol
Molar mass
119.1290g/mol
Density
1.1890g/cm3
Appearence

2-Aminocyclohepta-2,4,6-trien-1-one, also known as troponeimine, typically appears as a yellow crystalline solid. It has aromatic characteristics due to its conjugated ring structure, contributing to its distinctive appearance.

Comment on solubility

Solubility of 2-aminocyclohepta-2,4,6-trien-1-one

The solubility of 2-aminocyclohepta-2,4,6-trien-1-one is influenced by various factors, primarily due to its unique structure and functional groups. This compound, featuring both amino and keto functional groups, presents interesting solubility characteristics:

  • Polarity: The presence of the amino group can enhance solubility in polar solvents due to hydrogen bonding capabilities.
  • Solvent Compatibility: It is likely to be soluble in water and alcohols while exhibiting limited solubility in non-polar solvents like hexane.
  • Concentration Factors: Solubility may vary significantly with temperature and concentration; as the temperature increases, so might the solubility.

In summary, while 2-aminocyclohepta-2,4,6-trien-1-one demonstrates favorable solubility in polar environments, forming effective interactions with solvents, one must consider specific conditions that might further influence its behavior.

Interesting facts

Interesting Facts about 2-Aminocyclohepta-2,4,6-trien-1-one

2-Aminocyclohepta-2,4,6-trien-1-one is a fascinating organic compound with unique properties and structural features. Here are some intriguing aspects of this compound:

  • Structural Complexity: The molecule features a seven-membered cycloheptene ring, which contributes to its interesting conformational and electronic characteristics.
  • Functional Groups: It contains both an amino group and a ketone group, making it an example of a compound with diverse reactivity and potential applications in organic synthesis.
  • Potential Applications: Compounds with similar structures have garnered attention in medicinal chemistry for their potential roles in drug development, particularly in the design of new pharmaceuticals.
  • Resonance Structures: The presence of conjugated double bonds in this compound allows for various resonance structures, which can stabilize the molecule and influence its reactivity. This is a key feature in understanding its chemical behavior.
  • Research Interest: Studies on compounds like 2-aminocyclohepta-2,4,6-trien-1-one can provide insights into the mechanisms of organic reactions, including nucleophilic attacks and rearrangements.

As a student or scientist exploring the world of organic chemistry, compounds such as 2-aminocyclohepta-2,4,6-trien-1-one serve as excellent case studies for understanding structure-activity relationships and the impact of molecular features on chemical properties.

In the words of a renowned chemist, "The beauty of chemistry lies in the complexity of structures and the elegance of their interactions." This compound exemplifies that beauty, presenting a rich avenue for exploration in chemical research.

Synonyms
2-Amino-2,4,6-cycloheptatrien-1-one
6264-93-3
2-aminocyclohepta-2,4,6-trien-1-one
2-Aminotropone
2-Aminocyclohepta-2,4,6-trienone
2,4,6-CYCLOHEPTATRIEN-1-ONE, 2-AMINO-
1-Amino-2,4,6-cyclohepta-trien-1-one
33504-43-7
BRN 2204836
tropone, 2-amino-
4-14-00-00035 (Beilstein Handbook Reference)
SCHEMBL728071
CHEMBL3251332
DTXSID10955133
MFCD01734302
2-amino-2,4,6-cycloheptarien-1-one
AKOS006340625
2-Amino-2,4,6-cycloheptatriene-1-one
AS-62344
DB-346680
CS-0060480
F11661
EN300-1425960
Z1203578079