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Lutidine

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Identification
Molecular formula
C7H7NO4
CAS number
119-89-1
IUPAC name
2,3-dihydropyridine-2,6-dicarboxylic acid
State
State

This compound exists as a solid at room temperature. It forms part of a group of dihydropyridine derivatives which are frequently employed in various chemical synthesis applications. The solid state facilitates handling and measurement in laboratory conditions.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.00
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.00
General information
Molecular weight
155.13g/mol
Molar mass
155.1280g/mol
Density
1.4500g/cm3
Appearence

2,3-Dihydropyridine-2,6-dicarboxylic acid typically appears as a crystalline solid. This compound can form colorless or pale yellow crystals, depending on the level of impurities. Structurally related compounds often absorb moisture from the air and can appear as a powder.

Comment on solubility

Solubility of 2,3-Dihydropyridine-2,6-dicarboxylic Acid

2,3-Dihydropyridine-2,6-dicarboxylic acid (C7H7NO4), a bicyclic compound, demonstrates distinct solubility characteristics influenced by its carboxylic acid functional groups. Understanding its solubility profile is essential for its applications in various fields, including pharmaceuticals and organic synthesis.

Key Factors Influencing Solubility

  • Polarity: The presence of two carboxylic acid groups enhances the compound's polarity, allowing for better solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability of the carboxylic acids to form hydrogen bonds increases interactions with solvent molecules, further promoting dissolving behavior.
  • pH Dependence: The solubility may vary with changes in pH, as the ionization of carboxylic acid groups can influence the extent of dissolution in aqueous environments.

In summary, 2,3-dihydropyridine-2,6-dicarboxylic acid is likely to exhibit good solubility in polar solvents due to its inherent structural features. As a result, it plays a significant role in various chemical processes where solubility is a pivotal factor for usability.

Interesting facts

Interesting Facts about 2,3-Dihydropyridine-2,6-Dicarboxylic Acid

2,3-Dihydropyridine-2,6-dicarboxylic acid is a fascinating compound with a variety of implications in both synthetic and biological chemistry. Here are some intriguing facts about this compound:

  • Structural Versatility: This compound features a pyridine ring, a constituent of numerous natural and synthetic compounds, that exhibits unique reactivity patterns.
  • Biological Relevance: Pyridine derivatives are commonly found in various biologically active compounds, lending 2,3-dihydropyridine-2,6-dicarboxylic acid potential significance in drug discovery and development.
  • Synthetic Utility: The carboxylic acid functional groups present in the structure can serve as versatile building blocks for further chemical modifications, thus making this compound a relevant target in organic synthesis.
  • Research Applications: Ongoing studies have investigated its use as a ligand in coordination chemistry, potentially enhancing properties in catalysis and materials science.

As quoted in research circles, "Exploring the derivatives of nitrogen-containing heterocycles can lead to groundbreaking discoveries in medicinal chemistry." This quote encapsulates the excitement surrounding compounds like 2,3-dihydropyridine-2,6-dicarboxylic acid, emphasizing the importance of continued exploration and innovation in the realm of organic compounds.

In summary, 2,3-dihydropyridine-2,6-dicarboxylic acid is not just another compound; it represents a bridge between fundamental chemical research and practical applications in various fields, such as pharmacology and materials science.

Synonyms
2,3-dihydropyridine-2,6-dicarboxylic acid
dihydrodipicolinate
16052-12-3
2,3-di-H-dipicolinate
2,3-dihydrodipicolinic acid
SCHEMBL346874
CHEBI:48052
DTXSID50274254
UWOCFOFVIBZJGH-UHFFFAOYSA-N
2,6-Pyridinedicarboxylic acid, 2,3-dihydro-
Q27120920