Interesting facts
Interesting Facts about 2-sulfanylbenzoic acid
2-sulfanylbenzoic acid, also known as mercaptobenzoic acid, is a fascinating compound that combines the properties of both thiols and carboxylic acids. Here are some noteworthy aspects of this intriguing chemical:
- Functional Groups: This compound features a −SH (sulfanyl) group attached to a benzoic acid backbone. The presence of the thiol group grants it unique reactivity characteristics.
- Applications: 2-sulfanylbenzoic acid is utilized in the synthesis of various organic compounds and polymers. It also serves as an important precursor in the field of medicinal chemistry.
- Biological Activity: The compound exhibits significant biological activity, which makes it a subject of interest in pharmacological studies. Its thiol group is known to participate in redox reactions, potentially leading to useful therapeutic effects.
- Metal Binding: One of the remarkable features of 2-sulfanylbenzoic acid is its ability to chelate metals. This property is leveraged in various applications, including metal ion extraction and environmental remediation.
- pH Sensitivity: Being a carboxylic acid, the pH of its environment can significantly influence its behavior, particularly its solubility and reactivity. Adjustments to pH can alter the protonation state of the carboxylic acid, affecting its chemical interactions.
In summary, 2-sulfanylbenzoic acid is much more than just a simple organic compound. Its unique structural features and diverse applications make it a valuable subject for both industrial and academic research. Understanding its properties not only enriches the field of organic chemistry but also paves the way for innovations in materials science and medicinal applications.
Synonyms
Thiosalicylic acid
2-Mercaptobenzoic acid
147-93-3
2-Sulfanylbenzoic acid
o-Mercaptobenzoic acid
2-Thiosalicylic acid
o-Thiosalicylic acid
2-Carboxythiophenol
o-Sulfhydrylbenzoic acid
o-Benzoic acid thiol
o-Carboxythiophenol
Benzoic acid, 2-mercapto-
o-Mercaptobenzoesaeure
BENZOIC ACID, O-MERCAPTO-
Salicylic acid, 2-thio-
thiosalicylate
Thiophenol-2-carboxylic acid
2-Mercapto-benzoic acid
MFCD00004836
USAF KF-2
USAF XR-35
USAF EK-T-2805
UNII-CIP6LXN5XW
HSDB 2739
NSC 2184
EINECS 205-704-3
Pirosal (TN)
Thiocyl (TN)
NSC 660640
BRN 0508507
DTXSID4049032
CHEBI:59124
AI3-23963
CIP6LXN5XW
NSC-2184
NSC-660640
THIOSALICYLIC ACID [MI]
DTXCID5028958
NSC2184
4-10-00-00272 (Beilstein Handbook Reference)
THIOSALICYLIC ACID [WHO-DD]
Thiocyl
2-THIOSALICYLIC ACID [HSDB]
NSC660640
Benzoic acid, mercapto-
NCGC00018107-04
THIOSALICYLIC ACID [USP IMPURITY]
THIOSALICYLIC ACID (USP IMPURITY)
CAS-147-93-3
o-Mercaptobenzoesaeure [German]
thiolate
2-thiosalicylate
oCarboxythiophenol
2Carboxythiophenol
CPC-Thiosal
thiosalicyclic acid
oThiosalicylic acid
2-thiobenzoic acid
2Thiosalicylic acid
JKE
oBenzoic acid thiol
Thisosalicyilic acid
oMercaptobenzoesaeure
oMercaptobenzoic acid
2mercaptobenzoic acid
2-Mercaptobenzoicacid
2Sulfanylbenzoic acid
oSulfhydrylbenzoic acid
Salicylic acid, 2thio
o-mercapto benzoic acid
o-mercapto-benzoic-acid
Benzoic acid, 2mercapto
WLN: SHR BVQ
ortho-mercaptobenzoic acid
2-Sulfanylbenzoic acid #
Thiosalicylic acid, 97%
Thiosalicylic acid, 98%
SCHEMBL50376
MLS000069414
CHEMBL119888
DTXCID6022472
THIOSALICYLIC ACID [INCI]
HY-Y0102
STR00467
Tox21_113560
STL163871
AKOS000119389
Tox21_113560_1
AT20777
CS-W020627
DB14026
FM25082
NCGC00018107-01
NCGC00018107-02
NCGC00018107-03
NCGC00018107-05
NCGC00022652-03
SMR000059130
SY007814
M0054
NS00004703
EN300-20328
D08586
SBI-0653844.0001
Q1312775
BRD-K36998189-001-01-9
BRD-K36998189-001-03-5
F2191-0258
Z104477754
2-Thiosalicylic acid;2-Carboxybenzenethiol;2-Carboxythiophenol
Solubility of 2-Sulfanylbenzoic Acid
2-Sulfanylbenzoic acid (C7H6O2S), also known as mercaptobenzoic acid, exhibits unique solubility characteristics due to its functional groups. Understanding its solubility is essential for various applications in chemistry.
Overall, the solubility of 2-sulfanylbenzoic acid is a fascinating balance dictated by its molecular structure and external conditions. As with many compounds, understanding the interplay of these factors is crucial for successful application in chemical processes.