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Identification
Molecular formula
C16H13BNO6S2
CAS number
909389-20-0
IUPAC name
[3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid
State
State

The compound exists as a solid at room temperature, typically appearing as a crystalline powder with a color ranging from white to off-white.

Melting point (Celsius)
163.00
Melting point (Kelvin)
436.15
Boiling point (Celsius)
533.30
Boiling point (Kelvin)
806.45
General information
Molecular weight
421.31g/mol
Molar mass
421.3100g/mol
Density
1.5800g/cm3
Appearence

The compound is typically a solid at room temperature. The appearance can vary ranging from white to off-white crystalline powder.

Comment on solubility

Solubility of 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid

The solubility of 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid (C16H13BNO6S2) is influenced by several factors due to its complex structure, which includes both boronic acid and sulfonyl functionalities. Key points regarding its solubility include:

  • Polar Nature: The presence of sulfonyl groups contributes to the compound’s polar character, potentially enhancing its solubility in polar solvents.
  • Hydrogen Bonding: The way the molecule can form hydrogen bonds may affect its solubility in aqueous solutions.
  • Organic Solvents: This compound may be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) or ethanol due to its comparatively non-polar regions.
  • pH Sensitivity: The solubility can vary significantly with changes in pH, as boronic acids can form anionic species in more alkaline conditions.

In summary, the solubility of 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid is a multifaceted characteristic that could be tailored by adjusting solvent type and environmental conditions.

Interesting facts

Interesting Facts about 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid

3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid is a fascinating compound with intriguing applications in various fields, especially in chemistry and material science. Here are some engaging insights about this compound:

  • Versatile Reactivity: This boronic acid derivative is known for its versatility in organic synthesis. It can participate in various coupling reactions, making it valuable in creating complex organic molecules.
  • Biological Importance: Compounds like this one are often explored for their biological activities. They have been studied for potential applications in medicinal chemistry, particularly in developing pharmaceuticals that target specific biological pathways.
  • Role in Sensors: The unique structure of 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid enables its use in sensor technology. It can be used to detect sugars and other biomolecules due to its ability to form reversible complexes with them, making it a cornerstone in biosensor development.
  • Functional Materials: This compound can be incorporated into advanced materials, enhancing properties such as conductivity and reactivity. Its incorporation can lead to functionalized polymers which may find applications in electronic devices.
  • Environmental Impact: The potential of boronic acids in catalysis highlights their role in green chemistry. Their reactivity and low toxicity contribute to sustainable practices in chemical manufacturing.

In summary, 3-[[4-(benzenesulfonyl)-2-thienyl]sulfonylamino]phenyl]boronic acid is not just a compound but a multifaceted entity with a broad spectrum of applications across research and industry. Its role as a versatile reactant and its potential in biological and material science make it a compound worth exploring further!

Synonyms
3-(4-BENZENESULFONYL-THIOPHENE-2-SULFONYLAMINO)-PHENYLBORONIC ACID
CHEMBL113381
(3-(4-(benzenesulfonyl)thiophene-2-sulfonamido)phenyl)boronic acid
{3-[4-(benzenesulfonyl)thiophene-2-sulfonamido]phenyl}boronic acid
SCHEMBL4316537
BDBM50115616
DB02858
PD007576
NS00073529
Q27093820
[3-({[4-(phenylsulfonyl)thiophen-2-yl]sulfonyl}amino)phenyl]boronic acid
3-(4-benzene-sulphonyl-thiophene-2-sulphonylamino)-phenylboronic acid
4-Benzenesulfonyl-thiophene-2-sulfonic acid (3-dihydroxyboranyl-phenyl)-amide