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Quinine Sulfate

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Identification
Molecular formula
C40H50N4O8S
CAS number
207671-44-1
IUPAC name
(6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol;sulfuric acid
State
State

Quinine sulfate is typically found as a solid at room temperature.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
745.00
Boiling point (Kelvin)
1 018.15
General information
Molecular weight
782.96g/mol
Molar mass
782.9560g/mol
Density
1.2500g/cm3
Appearence

Quinine sulfate appears as a white crystalline powder. It is soluble in alcohol and very slightly soluble in water. The crystals can exhibit a slight sheen and are often lustrous under proper lighting.

Comment on solubility

Solubility of (6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol; sulfuric acid

The solubility of the compound (6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol can be influenced by a variety of factors, including polarity, molecular structure, and the presence of functional groups. In the case of this particular compound, the following aspects are noteworthy:

  • Polarity: The presence of both the quinoline and quinuclidine structures suggests a mixed polarity nature. These features often promote solubility in polar solvents.
  • Functional Groups: The methoxy and hydroxyl groups may enhance hydrogen bonding capabilities, increasing the solubility in polar solvents, including alcohols and water.
  • Conjugation Effects: The vinyl group can introduce additional conjugation, potentially enhancing solubility in organic solvents by allowing for better interaction with the solvent molecules.

When considering the solubility of the compound in sulfuric acid, it is particularly interesting due to the acid's strong polar nature. This could lead to the following possibilities:

  • Increased Solubility: Sulfuric acid's ability to ionize and form strong hydrated ions may assist in the dissolution of this compound.
  • Reactivity: Additionally, the compound may undergo protonation or other acid-base reactions in the presence of sulfuric acid, altering its solubility characteristics.

Overall, it is reasonable to predict that (6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol will show notable solubility in polar solvents, particularly in acidic solutions such as sulfuric acid, due to its complex structure and reactive functional groups.

Interesting facts

Interesting Facts about (6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol; sulfuric acid

The compound in question is a fascinating example of a dual-function molecule that showcases the intricate relationship between structure and function in chemistry. Here are some intriguing insights into its characteristics:

  • Structural Diversity: This compound comprises a quinoid structure, which is known for its potential **biological activities**. The presence of methoxy and vinyl groups can greatly influence the compound's interaction with biological targets.
  • Biological Significance: Compounds similar to this one have shown promise in pharmacological studies, particularly in fields related to neurology and psychiatry. They can serve as potential leads for the development of new **medications**.
  • Catalytic Behavior: The inclusion of sulfuric acid is significant, as it can act as a catalyst in various chemical reactions. Sulfuric acid is known for its ability to accelerate reactions, providing enhanced **reaction rates** and **yields** in organic synthesis.
  • Versatile Applications: The unique combination of components in this compound lends itself to a variety of applications, including in the fields of materials science and nanotechnology. Its diverse reactivity can be leveraged for synthesizing **novel materials**.
  • Research Interest: Scientists are increasingly interested in exploring compounds of this nature due to their potential in creating new **therapeutics** and as **probes** for biological studies.

In summary, (6-methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol; sulfuric acid highlights the exciting intersection of organic synthesis, drug development, and catalysis. Future research continues to unveil its potential, leading to advancements in both chemistry and medicine.

Synonyms
Quinidate
Quinine sulphate
Chinidine sulfate
Quinidine monosulfate
(5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl)-(6-methoxyquinolin-4-yl)methanol;sulfuric acid
GNF-PF-5473
Cin quin
(R)-(6-Methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methanol sulfate
SCHEMBL394497
CHEMBL197253
Cinchonan-9-ol, 6'-methoxy-, (8.alpha.,9R)-, sulfate (salt)
NSC-667852
NCGC00094774-01
NCGC00094774-02
DB-052667
NS00080353
A918193
Cinchonan-9-ol, (8.alpha.,9R)-, sulfate (2:1) (salt)
WLN: T66 BNJ HO1 EYQ- DT66 A B CNTJ G1U1 &WSQQ