Interesting facts
Interesting Facts About 4-Methoxybenzenesulfonyl Chloride
4-Methoxybenzenesulfonyl chloride, often referred to in shorthand as p-anisylsulfonyl chloride, is a fascinating compound that presents various applications and chemical characteristics worth highlighting. Here are some engaging facts:
- Key Functional Group: This compound features a sulfonyl chloride group, which makes it a reactive intermediates in organic synthesis. The sulfonyl chloride functionality is particularly useful for the introduction of sulfonyl groups into other organic molecules.
- Synthetic Applications: 4-Methoxybenzenesulfonyl chloride is often utilized in the synthesis of sulfonamides and can be employed for preparing derivatives of phenols. It is commonly used in drug development and materials science.
- Stability Considerations: Although the compound is stable under standard conditions, it can react vigorously with water, releasing hydrogen chloride gas. Thus, handling it requires appropriate safety measures; “Understanding the reactivity is crucial for safe laboratory practices.”
- Industrial Importance: Sulfonyl chlorides, including 4-methoxybenzenesulfonyl chloride, are utilized in the manufacture of dyes, pigments, and pharmaceuticals, showcasing their broad industrial significance.
- Solubility and Reactivity: This compound is generally soluble in organic solvents which makes it easy to work with in various organic reactions. The presence of the methoxy group provides both electron-donating properties and steric hindrance, enhancing its selectivity in reactions.
In conclusion, 4-methoxybenzenesulfonyl chloride is not only important for its functional versatility in organic synthesis but also serves as an excellent example of how small structural changes can significantly influence the chemical behavior of a compound. For anyone exploring the vast world of organic chemistry, understanding the nuances of sulfonyl chloride derivatives can open doors to novel pathways and reactions!
Synonyms
4-Methoxybenzenesulfonyl chloride
98-68-0
4-Methoxybenzene-1-Sulfonyl Chloride
Benzenesulfonyl chloride, 4-methoxy-
p-Anisylsulfonyl chloride
4-Methoxy-benzenesulfonyl chloride
4-Methoxybenzenesulphonyl chloride
MFCD00007446
P-METHOXYBENZENESULFONYL CHLORIDE
p-Methoxyphenylsulfonyl chloride
4-Methoxyphenylsulfonyl Chloride
Benzenesulfonyl chloride, p-methoxy-
EINECS 202-692-1
4-methoxybenzenesulfonic acid chloride
DTXSID50243364
4-(methyloxy)benzenesulfonyl chloride
NSC 403292
4-Methoxybenzenesulfonylchloride
p-Anisolesulfonyl Chloride
SCHEMBL67837
4-methoxyphenylsulfonylchloride
p-methoxybenzenesulfonylchloride
4methoxybenzenesulfonyl chloride
4-methoxybenzensulfonyl chloride
4-methoxybezenesulfonyl chloride
4-methoxybenzenesulphonylchloride
4-methoxy-benzenesulfonylchloride
4-methoxybenzene sulfonylchloride
4-methoxyphenylsulphonyl chloride
rho-methoxybenzenesulfonylchloride
4-methoxy-benzensulfonyl chloride
p-methoxybenzenesulphonyl chloride
DTXCID50165855
4-methoxy benzenesulfonyl chloride
4-methoxy- benzenesulfonylchloride
4-methoxybenzene sulfonyl chloride
4-methoxybenzene-sulfonyl chloride
4-methoxy-benzenesulphonyl chloride
4-methoxybenzene-sulphonyl chloride
4-methoxyl-benzenesulfonyl chloride
para-methoxybenzenesulfonyl chloride
4-(methoxy)benzenesulfonyl chloride
4-methoxy benzene sulfonyl chloride
4-methoxy-benzene sulfonyl chloride
4-methoxy benzene sulphonyl chloride
4-Methoxybenzene-1-SulfonylChloride
4-methoxyphenylsulfonic acid chloride
BBL010130
NSC403292
STL145904
AKOS000119609
CS-W004070
FM61107
NSC-403292
4-methoxy-benzenesulphonic acid chloride
4-Methoxybenzenesulfonyl chloride, 99%
AS-14044
BP-11911
DB-229178
M0802
NS00041416
EN300-17025
F11798
Z56860355
F0808-2032
202-692-1
p-Anisolesulfonyl Chloride;4-Methoxyphenylsulfonyl Chloride;4-Methoxybenzene-1-sulfonyl chloride
Solubility of 4-methoxybenzenesulfonyl chloride
The solubility of 4-methoxybenzenesulfonyl chloride in various solvents is an intriguing topic, particularly because this compound's behavior in solution can provide insights into its reactivity and application potential.
As a sulfonyl chloride, it is reactive and can participate in nucleophilic substitution reactions. Therefore, its solubility can greatly impact its reactivity:
In summary, the solubility behavior of 4-methoxybenzenesulfonyl chloride showcases a complex interplay between structure and solvent interactions, with notable implications for its usability in chemical synthesis.