Interesting facts
Interesting Facts about Prop-2-ynyl 4-Methylbenzenesulfonate
Prop-2-ynyl 4-methylbenzenesulfonate, commonly referred to in the scientific community for its unique properties and versatile applications, is a fascinating organic compound with a myriad of uses. Here are some intriguing insights:
- Functional Group Diversity: This compound features both an alkyne and a sulfonate functional group. The presence of these diverse functionalities allows for various chemical reactions and synthetic pathways, making it a valuable building block in organic synthesis.
- Reactivity: The alkyne group in prop-2-ynyl 4-methylbenzenesulfonate can participate in cycloaddition reactions, which are crucial for forming complex structures in pharmaceutical chemistry. It enables the formation of highly functionalized compounds through controlled reactions.
- Applications in Synthesis: This compound is often utilized in the synthesis of biologically active molecules, particularly in the development of new drugs and agrochemicals. Its ability to serve as a sulfonate leaving group makes it an essential reagent in nucleophilic substitution reactions.
- Role in Material Science: Due to its structural properties, prop-2-ynyl 4-methylbenzenesulfonate has potential applications in material science, including the development of polymers and inks, where its unique backbone can enhance stability and reactivity.
- Environmental Prospects: Research into the environmental impact of sulfonate esters, such as prop-2-ynyl 4-methylbenzenesulfonate, is ongoing, focusing on biodegradability and potential toxic effects, underscoring the importance of green chemistry.
In summary, prop-2-ynyl 4-methylbenzenesulfonate is not just a chemical compound; it is a versatile tool in the arsenal of chemists looking to innovate in organic synthesis, pharmaceuticals, and material science. As one researcher aptly put it, "Every molecule tells a story, and the stories of sulfonates are particularly compelling."
Synonyms
Propargyl p-toluenesulfonate
6165-76-0
2-Propyn-1-ol, 4-methylbenzenesulfonate
p-TOLUENESULFONIC ACID, 2-PROPYNYL ESTER
CCRIS 9146
BRN 1912957
XBC3GGJ44A
2-propynyl p-toluenesulfonate
DTXSID80210665
4-11-00-00263 (Beilstein Handbook Reference)
1-((P-TOLUENESULFONYL)OXY)-2-PROPYNE
DTXCID10133156
629-278-7
Prop-2-yn-1-yl 4-methylbenzenesulfonate
Propargyl Tosylate
prop-2-ynyl 4-methylbenzenesulfonate
Propargyl p-toluene sulfonate
MFCD01462194
p-Toluenesulfonic Acid Propargyl Ester
UNII-XBC3GGJ44A
Propargyl p-toluenesulphonate
SCHEMBL1117279
2-Propynyl 4-methylbenzenesulfonate #
AKOS015840418
AB10387
AC-7059
CS-W015112
AS-19271
SY025680
NS00123213
prop-2-yn-1-yl 4-methylbenzene-1-sulfonate
T1455
Propargyl p-toluenesulfonate, >=97.0% (GC)
EN300-5034481
Solubility of Prop-2-ynyl 4-methylbenzenesulfonate
Prop-2-ynyl 4-methylbenzenesulfonate, a compound with the formula C10H11O3S, exhibits discernible solubility characteristics that are noteworthy for various applications.
The solubility of this compound can be influenced by several factors, including:
In practice, it is important to consult solubility data for specific applications, as "like dissolves like" remains a fundamental principle in chemistry. As always, accurate testing is crucial to determine the exact solubility in different solvents and conditions.