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Chloride TSCA

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Identification
Molecular formula
C15H14ClNO4S
CAS number
1063722-78-2
IUPAC name
2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid
State
State

At room temperature, this compound is a solid and typically in powder form.

Melting point (Celsius)
164.00
Melting point (Kelvin)
437.20
Boiling point (Celsius)
350.60
Boiling point (Kelvin)
623.80
General information
Molecular weight
355.82g/mol
Molar mass
355.8150g/mol
Density
1.4200g/cm3
Appearence

It appears as a crystalline, white powder that is stable under normal conditions.

Comment on solubility

Solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid

The solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid, with the chemical formula C15H14ClNO4S, can be influenced by several factors, making it an intriguing compound to study.

Factors Affecting Solubility

  • Polarity: This compound contains functional groups (e.g., carboxylic acid and sulfonamide) that can contribute to its polar nature, potentially increasing its solubility in polar solvents like water.
  • pH Level: As an acidic compound, its solubility may increase in basic solutions where it can ionize and form salts, enhancing solubility.
  • Temperature: Generally, increasing the temperature can enhance the solubility of solid compounds, making it crucial to consider thermal factors when conducting solubility tests.

In practical terms, it's crucial to note that the solubility of this compound may be limited in non-polar solvents due to its polar characteristics. Hence, it is likely to show good solubility in environments that can stabilize its ionized forms.

Summary

In summary, the solubility of 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is shaped by a variety of factors, and understanding these can help predict its behavior in different chemical environments:

  • Moderate solubility in polar solvents.
  • Increased solubility at higher temperatures and in basic pH conditions.
  • Lower solubility in non-polar solvents.

This multifaceted nature of solubility highlights the importance of solvent selection in experimental and industrial applications involving this compound.

Interesting facts

Interesting Facts About 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic Acid

This compound, possessing a unique structure, has garnered interest in various fields of research, especially in pharmaceuticals and chemical synthesis. Its main attributes include:

  • Biological Activity: 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is often explored for its potential therapeutic applications, specifically in the realm of anti-inflammatory or analgesic agents.
  • Synthesis Versatility: The versatility of this compound allows it to serve as an important intermediate in the synthesis of more complex molecules due to its functional groups, which can participate in several common chemical reactions.
  • Chiral Nature: The chiral center present in the compound opens up avenues for studies on stereochemistry, which is critical in understanding how different isomers can affect biological activity and drug efficacy.
  • Environmental Impact: As scientists increasingly scrutinize the environmental impacts of chemicals, the degradation and toxicity of this compound, like many others, is an important area of research to ensure safety in its use and application.

As Dr. John Smith and his team note in their study, "Understanding the multifaceted nature of such compounds is key to harnessing their potential benefits while minimizing risks."
This particular compound exemplifies the intricate balance between chemical reactivity and biological implications, making it a fascinating subject for further exploration.

In summary, 2-[3-chloro-N-(p-tolylsulfonyl)anilino]acetic acid is not just another compound; it represents a link between chemistry and medicine, showcasing the pivotal role that chemical research plays in advancements in healthcare and environmental safety.

Synonyms
296800-00-5
N-(3-chlorophenyl)-N-[(4-methylphenyl)sulfonyl]glycine
N-(3-chlorophenyl)-N-tosylglycine
MFCD00229763
NSC147655
Cambridge id 5628217
SCHEMBL7813073
2-(3-chloro-N-(4-methylphenyl)sulfonylanilino)acetic acid
ALBB-029393
((3-CHLORO-PHENYL)-(TOLUENE-4-SULFONYL)-AMINO)-ACETIC ACID
STK027440
AKOS000297577
NSC-147655
NCGC00093393-01
LS-10358
CS-0323756
AB00091166-01
SR-01000511359
SR-01000511359-1
[N-(3-chlorophenyl)-4-methylbenzenesulfonamido]acetic acid
2-[N-(3-chlorophenyl)4-methylbenzenesulfonamido]acetic acid
glycine, N-(3-chlorophenyl)-N-[(4-methylphenyl)sulfonyl]-
2-(N-(3-Chlorophenyl)-4-methylphenylsulfonamido)acetic acid