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Ethchlorvynol

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Identification
Molecular formula
C7H10ClNO
CAS number
522-29-0
IUPAC name
(5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride
State
State

At room temperature, Ethchlorvynol in its pure form typically exists as a solid powder. It is not volatile and tends to be stable under normal conditions of use and storage.

Melting point (Celsius)
40.00
Melting point (Kelvin)
313.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
267.16g/mol
Molar mass
267.1600g/mol
Density
1.2705g/cm3
Appearence

The compound is typically found in the form of a crystalline powder. It is usually a white to off-white solid, and its chloride salt form is commonly available in pharmaceutical preparations.

Comment on solubility

Solubility of (5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride

The solubility of *(5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride* can be categorized based on its ionic nature and structural components. Here are some key points regarding its solubility:

  • Ionic Compound: As a quaternary ammonium salt, this compound is likely to be soluble in polar solvents such as water due to the presence of ionic bonds.
  • Hydrophobic Influence: The *5-bromobenzothiophen* moiety contributes a hydrophobic region, which may diminish solubility in highly polar solvents.
  • Temperature Effects: Like many ionic compounds, solubility may increase with temperature, thus careful consideration of temperature during dissolution is recommended.
  • Solvent Choice: While water is a primary solvent for ionic compounds, *this specific compound might show better solubility in organic solvents* such as ethanol or methanol, which can stabilize both ionic and hydrophobic regions.

In conclusion, predicting the solubility of *(5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride* requires an understanding of both its ionic characteristics and hydrophobic influences. Further empirical testing in different solvents will provide a comprehensive understanding of its solubility behavior.

Interesting facts

Interesting Facts about (5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride

This fascinating compound, often used in the realm of medicinal chemistry, showcases a unique combination of bromobenzothiophene and ammonium functionalities. Here are some intriguing aspects that highlight its significance:

  • Structural Diversity: The compound features a bromobenzothiophene core, which is a noteworthy structure in organic chemistry known for its relevance in pharmaceutical applications.
  • Bioactivity: Compounds of this type have been studied for their potential biological activities, including anti-cancer properties. The thiophene ring is particularly interesting due to its role in drug development.
  • Ion Pairing: Being a quaternary ammonium salt, the presence of the chloride ion contributes to its solubility and bioavailability, making it a candidate for various therapeutic uses.
  • Synthetic Applications: The synthesis of this compound often involves novel synthetic routes, making it a valuable teaching example for students learning about multi-step synthesis techniques.
  • Versatile Reactivity: This compound can participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, expanding its utility in organic synthesis.

As a scientist exploring this compound, it's crucial to appreciate not only its structure and properties but also its potential impact in fields such as medicinal chemistry and drug development. Its unique composition encourages further study, including exploring modifications that could enhance its biological efficacy or reduce toxicity.

Furthermore, the exploration of quaternary ammonium compounds continues to offer insights into their roles in biological systems and material science. As you delve deeper into the world of (5-bromobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride, the possibilities for research and discovery are vast!

Synonyms
Benzo(b)thiophene-3-methylamine, 5-bromo-N-(2-chloroethyl)-N-ethyl-, hydrochloride
7349-46-4
5-Bromo-N-(2-chloroethyl)-N-ethylbenzo(b)thiophene-3-methylamine hydrochloride