Skip to main content

Methyl 2-mercaptobenzoate

ADVERTISEMENT
Identification
Molecular formula
C8H8O2S
CAS number
3071-32-7
IUPAC name
methyl 2-sulfanylbenzoate
State
State

At room temperature, methyl 2-mercaptobenzoate is in the liquid state, typically seen as a clear to slightly yellow liquid.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
263.00
Boiling point (Kelvin)
536.15
General information
Molecular weight
168.21g/mol
Molar mass
168.2130g/mol
Density
1.2897g/cm3
Appearence

Methyl 2-mercaptobenzoate appears as a pale yellow to brown liquid, which can have an aromatic odor characteristic of esters.

Comment on solubility

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:

  • Solubility in Organic Solvents: Methyl 2-sulfanylbenzoate is soluble in most organic solvents such as ethanol, methanol, and acetone.
  • Solubility in Water: Its solubility in water is very limited, suggesting a lipophilic nature due to its aromatic structure and sulfur component.

Influencing Factors

The solubility of methyl 2-sulfanylbenzoate can be influenced by various factors:

  • Temperature: Increasing temperature typically enhances solubility in organic solvents.
  • pH of the Solution: The presence of acidic or basic conditions in the solvent can affect the ionization of the compound, thereby influencing its solubility.

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!"

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