1-(Benzothiophen-3-yl)-2-morpholiniom-4-yl-ethanol chloride

Identification

Molecular formula

C₁₅H₂₂ClNOS

CAS number

.-46-272

IUPAC name

1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride

State

At room temperature, the compound exists as a solid. It is generally stable under standard conditions if stored properly.

Melting point (Celsius)

180.00

Melting point (Kelvin)

453.15

Boiling point (Celsius)

290.00

Boiling point (Kelvin)

563.15

General information

Molecular weight

309.84g/mol

Molar mass

309.8400g/mol

Density

1.2500g/cm³

Appearence

The compound typically appears as a white to off-white crystalline powder. Its purity and handling conditions can result in slight variations in color and texture.

Comment on solubility

Solubility of 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride

The solubility of 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride is influenced by several factors associated with its chemical structure.

Key Factors in Solubility

Polarity: The presence of the morpholine functional group introduces significant polarity, which generally enhances solubility in polar solvents.
Hydrogen Bonding: The hydroxyl (-OH) group contributes to the ability of the compound to engage in hydrogen bonding, further increasing its solubility in water.
Charge: As a quaternary ammonium salt, the chloride ion introduces ionic character which generally favors solubility in polar solvents like water.

Overall, one can expect that this compound is likely to be well soluble in polar solvents such as water and alcohols. However, it may show limited solubility in non-polar solvents, due to its ionic nature and polar functional groups.

Conclusion

In summary, the solubility of 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride can be described as:

High solubility in polar solvents
Low solubility in non-polar solvents

This property makes it a versatile compound for various applications, particularly in aqueous environments.

Interesting facts

Exploring 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride

The compound 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride is a fascinating example of how organic chemistry can interweave various molecular structures to create compounds with unique properties and functionalities. Below are some key aspects that make this compound notable:

Hybrid Structure: This compound features a morpholine ring, a six-membered heterocycle containing oxygen and nitrogen, combined with a benzothiophene moiety. This combination may influence its reactivity and biological activity.
Biological Applications: The presence of both the benzothiophene and morpholine structures suggests potential pharmacological properties. Compounds with such structures are often studied for their anti-cancer and anti-inflammatory effects.
Ionic Nature: The chloride ion in this compound highlights its salt-like characteristics, potentially making it more soluble and bioavailable in physiological environments.
Research Interest: Due to the unique structure, this compound is a subject of interest in medicinal chemistry and materials science, where its properties can be tailored for specific applications.
Potential Synthesis Routes: Chemists often explore various synthetic pathways to create compounds like this one, including methods like coupling reactions and nucleophilic substitutions, enhancing their understanding of reaction mechanisms.

The job of a chemist is to unravel the mysteries of such compounds, understanding their potential and harnessing it for various applications. As Thomas Edison once said, “There is a way to do it better—find it.” The synthesis and exploration of 1-(benzothiophen-3-yl)-2-morpholin-4-ium-4-yl-ethanol;chloride is yet another testament to the ingenuity of scientific inquiry.

Synonyms

alpha-(Morpholinomethyl)benzo(b)thiophene-3-methanol hydrochloride

7388-09-2

BENZO(b)THIOPHENE-3-METHANOL, alpha-(MORPHOLINOMETHYL)-, HYDROCHLORIDE