Skip to main content

Homopiperonycin

ADVERTISEMENT
Identification
Molecular formula
C40H36N4O10
CAS number
11122-64-8
IUPAC name
[2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate
State
State

The compound is a solid at room temperature. Its structure makes it stable, and it is usually stored in airtight containers to prevent degradation or reactions with moisture in the air.

Melting point (Celsius)
219.00
Melting point (Kelvin)
492.15
Boiling point (Celsius)
639.00
Boiling point (Kelvin)
912.15
General information
Molecular weight
795.81g/mol
Molar mass
795.8100g/mol
Density
1.3580g/cm3
Appearence

The compound appears as a white crystalline solid, which may be slightly off-white depending on the purity and form. It is typically found in the form of powder or small crystals.

Comment on solubility

Solubility of [2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate

The solubility of the compound [2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate can be influenced by several factors:

  • Polarity: The presence of hydroxyl groups and carboxylate moieties generally increases polarity, which may enhance solubility in polar solvents, such as water.
  • Functional Groups: The multiple pyridine rings contribute to the overall solubility profile, likely making the compound more soluble in organic solvents due to favorable π-π stacking interactions.
  • Temperature: Like many organic compounds, solubility may increase with temperature; thus, conducting experiments at higher temperatures could yield different solubility results.
  • pH Sensitivity: Given the presence of the carboxylate group, the solubility may be pH-sensitive, showing increased solubility in basic conditions where deprotonation occurs.

It is crucial to note that the solubility can be significantly variable and may require experimental determination under various conditions to obtain accurate data. Therefore, one should always refer to empirical solubility data when available, as theoretical predictions might not fully capture the complexities of solvation for such a multifunctional compound.

Interesting facts

Interesting Facts about [2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate

This compound, with its complex structure, is a fascinating example of synthetic organic chemistry. Often used in advanced research, it has several notable features:

  • Versatile Building Block: The compound serves as a versatile building block for the synthesis of more complex molecules, making it valuable in drug discovery and materials science.
  • Chelating Properties: Thanks to the presence of multiple pyridine rings, this compound can form chelates with metal ions, which is crucial in catalysis and coordination chemistry.
  • Pyridine Influence: Pyridine rings in the structure contribute significantly to its chemical reactivity, allowing for various substitution reactions that can tailor the compound's properties for specific applications.
  • Biological Applications: Some derivatives of similar compounds have shown promising biological activities, including antibacterial and antifungal properties, suggesting potential pharmaceutical applications.
  • Polymer Science: This compound's structure might also find use in creating specialized polymers with tailored functionalities for emerging technologies.

As with many compounds in organic synthesis, understanding its structure leads to insights into its function. As stated by renowned chemists, "The more complex the structure, the greater the potential for innovation." With compounds like this, the world of chemistry continuously expands, revealing new possibilities and advancements.

In conclusion, [2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate embodies the potential of a seemingly simple organic molecule to impact various fields, ranging from medicinal chemistry to materials science.

Synonyms
Nicomol
27959-26-8
Cholexamin
Nicomolum
2,2,6,6-Tetrakis(nicotinoyloxymethyl)cyclohexanol
215U8X2R44
RefChem:927731
(2-Hydroxycyclohexane-1,1,3,3-tetrayl)tetramethyl tetranicotinate
2-hydroxy-1,1,3,3,-cyclohexatetramethanol-1,1,3,3-tetranicotinate
248-748-9
Cholexamine
K 31 (pharmaceutical)
Nicomolol
(2-Hydroxycyclohexane-1,1,3,3-tetrayl)tetrakis(methylene) tetranicotinate
K 31
[2-hydroxy-1,3,3-tris(pyridine-3-carbonyloxymethyl)cyclohexyl]methyl pyridine-3-carboxylate
DTXSID9048722
NCGC00182074-02
2-Hydroxy-1,1,3,3-cyclohexanetetramethanol 1,1,3,3-tetranicotinate
DTXCID2028648
Nicomol [INN:JAN]
Nicomolum [INN-Latin]
CAS-27959-26-8
EINECS 248-748-9
BRN 0469260
Nicole Moore
UNII-215U8X2R44
Cholexamin (TN)
Cholexamin; Cholexamine
NICOMOL [INN]
NICOMOL [JAN]
NICOMOL [MI]
NICOMOL [MART.]
Tetranicotinic acid 2-hydroxycyclohexa-1,1,3,3-tetramethyl ester
Nicomol (JP18/INN)
NICOMOL [WHO-DD]
2-Hydroxycyclohexane-1,1,3,3-tetramethanol tetraester with nicotinic acid
3-Pyridinecarboxylic acid, (2-hydroxy-1,3-cyclohexanediylidene)tetrakis(methylene) ester
Nicotinic acid, 1,1,3,3-tetraester with 2-hydroxy-1,1,3,3-cyclohexanetetramethanol
SCHEMBL26713
orb1703029
CHEMBL2103919
SCHEMBL31423786
CHEBI:31904
VRAHPESAMYMDQI-UHFFFAOYSA-N
BCP23020
Tox21_113136
AKOS016014053
Tox21_113136_1
NCGC00182074-03
DA-56171
FH176231
HY-121776
CS-0083284
NS00049213
D01291
959N268
SR-01000883969
SR-01000883969-1
Q27253520
3-Pyridinecarboxylic acid (2-hydroxy-1,3-cyclohexanediylidene)tetrakis(methylene) ester
3-Pyridinecarboxylic acid,(2-hydroxy-1,3-cyclohexanediylidene)tetrakis(methylene) ester