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Identification
Molecular formula
C21H20N2O3
CAS number
123456-78-9
IUPAC name
1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid
State
State

At room temperature, it is typically found in a solid state, specifically as white to off-white crystalline powder.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
333.38g/mol
Molar mass
333.3840g/mol
Density
1.1963g/cm3
Appearence

The compound is generally a white to off-white crystalline powder.

Comment on solubility

Solubility of 1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid (C21H20N2O3)

The solubility of 1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid is influenced by various factors, making it an intriguing compound for study:

  • Polarity: The presence of functional groups such as carboxylic acid can contribute to polar characteristics, potentially enhancing solubility in polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds, especially due to the –COOH (carboxylic acid) and –NH (amine) groups, might suggest increased solubility in aqueous solutions.
  • Solvent Characteristics: This compound is likely to be more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), which can stabilize non-polar parts of the molecule.
  • Temperature Influence: As with many organic compounds, an increase in temperature may improve solubility, enabling more effective dissolution processes.

While specific solubility data may be limited, it is essential to consider these factors when evaluating the solubility behavior of this compound. Understanding the solubility is crucial for applications in pharmaceuticals and material sciences, where solubility can determine bioavailability and reactivity.

Interesting facts

Interesting Facts about 1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid

This compound, known for its complex structure, represents an intersection of organic and medicinal chemistry. Here are some fascinating aspects that you might find intriguing:

  • Unique Structure: The molecular architecture includes a pyridine ring fused with a carboxylic acid group, which contributes to its reactivity and interaction with biological molecules.
  • Biological Relevance: Compounds with similar structures have been studied for their potential in pharmacological applications, including anti-cancer and anti-inflammatory properties.
  • Mechanism of Action: Its design suggests possible interactions with specific enzymes or receptors, making it a candidate for research in drug development.
  • Versatile Functional Groups: The presence of both amino and carboxylic acid groups can facilitate various reactions, including synthesis of derivatives or conjugates, enhancing its utility in the lab.
  • Chemistry at Play: The compound can participate in reactions such as amide formation or esterification, which opens up avenues for further functionalization.

Interestingly, a noteworthy quote from a chemist may sum up the intrigue surrounding such compounds: "In chemistry, it's not just about structure—it's about the stories that molecules tell through their reactions and interactions." This highlights the importance of understanding the relationships between structure and function in the realm of chemical research.

Overall, the exploration of 1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid not only enhances our knowledge of organic compounds but also paves the way for innovative solutions in medicinal chemistry.

Synonyms
159094-94-7
NO-711
Nnc-711
BGU9MZ2G30
1-(2-{[(diphenylmethylidene)amino]oxy}ethyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid
3-Pyridinecarboxylic acid, 1-(2-(((diphenylmethylene)amino)oxy)ethyl)-1,2,5,6-tetrahydro-
CHEMBL473104
1-[2-(benzhydrylideneamino)oxyethyl]-3,6-dihydro-2H-pyridine-5-carboxylic acid
1-(2-(((Diphenylmethylene)amino)oxy)ethyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid
CHEMBL545050
1-(2-(((Diphenylmethylene)amino)oxy)ethyl)-1,2,5,6-tetrahydropyridine-3-carboxylicacid
3-Pyridinecarboxylic acid, 1-[2-[[(diphenylmethylene)amino]oxy]ethyl]-1,2,5,6-tetrahydro-
UNII-BGU9MZ2G30
Tocris-1779
Lopac-N-142
Biomol-NT_000271
Lopac0_000880
BPBio1_000948
GTPL4669
SCHEMBL5969062
CHEBI:92744
DTXSID30166582
HMS3752K11
BDBM50080344
BDBM50426075
CCG-204962
SDCCGSBI-0050855.P002
NCGC00015712-01
NCGC00015712-02
NCGC00015712-03
NCGC00015712-04
NCGC00015712-05
NCGC00015712-08
NCGC00025293-01
NCGC00025293-02
NCGC00025293-03
HY-114040
CS-0064919
BRD-K42221274-001-01-4
BRD-K42221274-003-02-8
BRD-K42221274-003-07-7
Q27891706
1,2,5,6-tetrahydro-1-[2-[[(diphenylmethylene)amino]oxy]ethyl]-3-pyridinecarboxylic acid
1-(2-Benzhydrylideneaminooxy-ethyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid; hydrochloride
9BC