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Dimethylpyrrolidinium bromide

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Identification
Molecular formula
C18H20BrNO3S
CAS number
Not available
IUPAC name
(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate;bromide
State
State

The compound is typically solid at room temperature, reflecting its crystalline structure and physical characteristics.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
367.27g/mol
Molar mass
367.2730g/mol
Density
1.2940g/cm3
Appearence

The compound typically appears as a crystalline solid. The crystalline nature gives it a definitive structure, often manifesting in a white color.

Comment on solubility

Solubility Characteristics of (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate;bromide

The solubility of the compound (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate; bromide can be an intriguing subject due to its unique structure. Understanding solubility is crucial for predicting how this compound will behave in various environments. Here are some key points to consider:

  • Polarity: The presence of both polar and non-polar groups in this compound suggests that it may have moderate solubility in polar solvents such as water, while also showing better solubility in organic solvents.
  • Hydrogen Bonding: The hydroxyl group in the structure can engage in hydrogen bonding, potentially enhancing the solubility in polar solvents.
  • Salt Formation: As a bromide salt, it may exhibit different solubility characteristics than its neutral form. Bromide salts are generally soluble in water, providing an interesting contrast.
  • Structural Complexity: The intricate arrangement of the thienyl and phenyl groups could influence the overall solubility due to steric hindrance or electronic effects.

As a general rule of thumb, "like dissolves like." Thus, the combination of polar and non-polar regions in this compound may mean it is soluble in both polar and non-polar solvents, but its exact solubility profile will depend on the concentration and temperature of the solvent.

In conclusion, while specific solubility data may require empirical measurement, the analysis of the compound's structural features provides valuable insights into its potential behavior in various solvents. Understanding these aspects can guide researchers in applications where solubility is a critical factor.

Interesting facts

Interesting Facts about (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate; bromide

(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate; bromide is a fascinating compound that has garnered interest within the realms of organic chemistry and pharmacology. Below are some notable aspects of this intriguing substance:

  • Structure and Function: The compound features a unique pyrrolidin-ium core, which is a saturated heterocycle containing a nitrogen atom, contributing to its positive charge and distinctive chemical reactivity.
  • Biological Potential: Compounds that contain both thienyl and phenolic moieties often exhibit interesting biological activities, including antioxidant properties. This suggests potential applications in medicinal chemistry.
  • Quaternary Ammonium Ion: The presence of a quaternary ammonium ion in the structure can enhance solubility and permeability across biological membranes, making it a point of interest for drug design.
  • Applications in Research: Its unique structure allows researchers to explore its behavior in various chemical environments, particularly in organic synthesis and the development of new materials.
  • Ion Pair Formation: The bromide counterion can influence the solubility and stability of the compound, making it relevant in formulating drug delivery systems.

In summary, (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-(2-thienyl)acetate; bromide is more than just a chemical formula. It embodies a wealth of potential applications, intriguing chemical behavior, and opportunities for advanced research in both the academic and pharmaceutical fields.

Synonyms
HETERONIUM BROMIDE
Hetrum bromide
7247-57-6
Bromure d'heteronium
Bromuro de heteronio
B41610WX8O
Pyrrolidinium, 3-((hydroxyphenyl-2-thienylacetyl)oxy)-1,1-dimethyl-, bromide
Heteronii bromidum
Heteronii bromidum [INN-Latin]
Bromure d'heteronium [INN-French]
Bromuro de heteronio [INN-Spanish]
LY 31814
UNII-B41610WX8O
Heteronium bromide [USAN:INN:BAN]
1-Methyl-3-pyrrolidyl phenyl-2-thienylglycolate methobromide
1,1-Dimethyl-3-(alpha-(2-thienyl)mandeloyloxy)pyrrolidinium bromid
(+-)-3-Hydroxy-1,1-dimethylpyrrolidinium bromide alpha-phenyl-2-thiopheneglycolate
alpha+beta-(+-)-(1-Methyl-3-pyrrolidinyl) alpha-phenyl-alpha-(2-thienyl)glycolate methobromide
SCHEMBL668862
HETERONIUM BROMIDE [MI]
CHEMBL2106335
Heteronium bromide (USAN/INN)
HETERONIUM BROMIDE [INN]
DTXSID20993288
HETERONIUM BROMIDE [USAN]
(+/-)-HETERONIUM BROMIDE
HAA24757
Pyrrolidinium, 3-hydroxy-1,1-dimethyl-, bromide, alpha-phenyl-2-thiopheneglycolate
NS00122212
D04434
Q27274331
(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-hydroxy-2-phenyl-2-thiophen-2-ylacetate;bromide
3-{[Hydroxy(phenyl)(thiophen-2-yl)acetyl]oxy}-1,1-dimethylpyrrolidin-1-ium bromide
(+/-)-3-HYDROXY-1,1-DIMETHYLPYRROLIDINIUM BROMIDE .ALPHA.-PHENYL-2-THIOPHENEGLYCOLATE
.ALPHA.+.BETA.-(+/-)-(1-METHYL-3-PYRROLIDINYL) .ALPHA.-PHENYL-.ALPHA.-(2-THIENYL)GLYCOLATE METHOBROMIDE
PYRROLIDINIUM, 3-((2-HYDROXY-2-PHENYL-2-(2-THIENYL)ACETYL)OXY)-1,1-DIMETHYL-, BROMIDE (1:1)