Interesting facts
Interesting Facts about Methyl 2-sulfanylbenzoate
Methyl 2-sulfanylbenzoate, often referred to in specialized circles as a compound of significant interest, belongs to the category of benzoate esters. This compound is particularly noteworthy for a variety of reasons:
- Biological Relevance: Methyl 2-sulfanylbenzoate holds potential biological activity, making it a candidate for further investigation in medicinal chemistry. Compounds featuring sulfur are often responsible for various biochemical functions, adding to its allure.
- Synthesis Techniques: The synthesis of this ester can involve various methodologies, typically relying on the reaction between benzoic acid derivatives and methylating agents. Such procedures are a staple in organic chemistry, fostering a deeper understanding of ester formation.
- Fragrance Component: Methyl 2-sulfanylbenzoate can be employed in the fragrance industry. Sulfur-containing compounds are known for their distinctive aromas, enhancing their value in perfumery and flavoring.
- Research Applications: In the realm of materials science, this compound is being explored for its potential applications in the development of new materials and as a chemical intermediate for various synthetic pathways.
As a student or scientist delving into the world of organic compounds, one might reflect on the following quote by a renowned chemist:
“Chemistry is the study of transformation, and each compound tells a story of its own.”
Exploring compounds like methyl 2-sulfanylbenzoate highlights the intricate web of chemical interactions and the potential for new discoveries. Its diverse applications ranging from functional pharmacology to creative fragrance design reflect the vast scope of organic chemistry.
Synonyms
Benzoic acid, 2-mercapto-, methyl ester
Methyl thiosalicylate
Methyl 2-mercaptobenzoate
4892-02-8
Methyl 2-sulfanylbenzoate
Methyl o-mercaptobenzoate
methyl-2-mercaptobenzoate
USAF MA-15
MFCD00060678
2-(Methoxycarbonyl)thiophenol
BENZOIC ACID, o-MERCAPTO-, METHYL ESTER
2-Mercaptobenzoic Acid Methyl Ester
NSC-30156
Methyl-o-mercaptobenzoate
NSC 30156
BRN 0956859
2-carbomethoxythiophenol
Methyl ar-thiosalicylate
2-carbmethoxy thiophenol
AI3-26181
methyl 2-mercapto-benzoate
WLN: 1SVR
Methyl 2-sulfanylbenzoate #
Methyl thiosalicylate, 97%
SCHEMBL212175
2-(Methoxycarbonyl)benzenethiol
66T62U8QUZ
Thiosalicylic Acid Methyl Ester
DTXSID30863468
2-Mercapto- benzoicacid-methylester
NSC30156
2-mercapto-benzoic acid methyl ester
AKOS009166691
CS-W017801
DS-3262
SY025573
M1881
EN300-29831
A10543
4-10-00-00280 (Beilstein Handbook Reference)
InChI=1/C8H8O2S/c1-10-8(9)6-4-2-3-5-7(6)11/h2-5,11H,1H
Solubility of Methyl 2-sulfanylbenzoate
Methyl 2-sulfanylbenzoate, with the chemical formula C9H10O2S, exhibits interesting solubility characteristics that are worth noting.
Solubility in Common Solvents
This compound is generally soluble in organic solvents. Here are some specifics:
Influencing Factors
The solubility of methyl 2-sulfanylbenzoate can be influenced by various factors:
Conclusion
In summary, while methyl 2-sulfanylbenzoate displays limited solubility in water, its good solubility in various organic solvents makes it a versatile compound for chemical applications. Remember, "Understanding solubility is key to mastering chemical interactions!"