Skip to main content

Clomeprop

ADVERTISEMENT
Identification
Molecular formula
C9H9ClO2S
CAS number
3917-03-9
IUPAC name
2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid
State
State

At room temperature, Clomeprop is a solid substance. It is typically stable and does not readily evaporate under standard conditions.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
465.30
Boiling point (Kelvin)
738.45
General information
Molecular weight
202.68g/mol
Molar mass
202.6730g/mol
Density
1.2489g/cm3
Appearence

Clomeprop appears as a crystalline powder. It may vary in color from white to off-white, depending on purity and specific forms. It is typically odorless or may have a mild characteristic odor.

Comment on solubility

Solubility of 2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid

The solubility of 2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid can be quite intriguing due to its complex structure, which impacts how it interacts with solvents. This compound is likely to exhibit varying solubility characteristics based on the following factors:

  • Polarity: The presence of functional groups such as the sulfanyl (-SH) and carboxylic acid (-COOH) contributes to polar interactions, which may enhance solubility in polar solvents like water.
  • Hydrophobic Interactions: The chlorophenyl structure can introduce hydrophobic characteristics, potentially limiting solubility in water but enhancing solubility in organic solvents like ethanol or acetone.
  • Temperature: Solubility often increases with temperature; thus, higher temperatures may help dissolve this compound more readily.
  • pH Levels: The acid nature of the compound may lead to changes in solubility based on the pH of the environment, where an increase in pH may deprotonate the carboxylic acid, improving solubility in basic solutions.

Overall, while 2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid may show considerable solubility in certain solvents, attention to the specific conditions and media is essential for predicting its behavior. As a general observation, this compound could be expected to have a higher solubility in organic solvents than in pure water due to its unique polar and hydrophobic properties.

Interesting facts

Interesting Facts about 2-(4-Chloro-2-methyl-phenyl)sulfanylacetic Acid

2-(4-Chloro-2-methyl-phenyl)sulfanylacetic acid is a fascinating compound that showcases the intricate world of organic chemistry. Here are some interesting aspects of this compound:

  • Functional Groups: This compound contains a sulfanyl group and a carboxylic acid functional group, making it a unique example of a thiol derivative. The presence of these groups often influences the compound's reactivity and interactions with biological systems.
  • Chirality and Isomers: The presence of chiral centers in its structure may lead to the existence of different stereoisomers. Studying these isomers is crucial for understanding their distinct chemical behaviors and biological activities.
  • Biological Significance: Compounds similar to this one have been studied for their potential biological activities, including antimicrobial and anti-inflammatory properties. Understanding the structure-activity relationship can help in drug design and therapeutic applications.
  • Applications in Synthesis: The sulfanyl group can serve as a versatile building block in organic synthesis, allowing chemists to create a variety of functionalized compounds. Its reactivity towards electrophiles can lead to the formation of new bonds, expanding the possibilities for synthesis in medicinal chemistry.

As elucidated by renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." The exploration of 2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid encourages innovative thoughts and opens doors to myriad avenues of chemical research.

Overall, this compound not only serves as an intriguing subject for study but also highlights the intricate connections between structure, properties, and functions in the chemical universe.

Synonyms
Red 3B Acid
94-76-8
Chlorotolylthioglycolic acid
(4-Chloro-o-tolylmercapto)acetic acid
Acetic acid, [(4-chloro-2-methylphenyl)thio]-
((4-Chloro-o-tolyl)thio)acetic acid
4-Chloro-2-methylphenylthioglycolic acid
HSDB 2671
Acetic acid, ((4-chloro-o-tolyl)thio)-
((4-Chloro-2-methylphenyl)thio)acetic acid
EINECS 202-362-7
(4-Chloro-2-methylbenzenemercapto)acetic acid
4-CHLORO-O-TOLYLTHIOACETIC ACID
Acetic acid, ((4-chloro-2-methylphenyl)thio)-
BRN 2526465
Acetic acid, 2-((4-chloro-2-methylphenyl)thio)-
AI3-26885
2-(4-chloro-2-methylphenyl)sulfanylacetic acid
I66W18916F
[(4-CHLORO-2-METHYLPHENYL)THIO]ACETIC ACID
4-06-00-02030 (Beilstein Handbook Reference)
4-CHLORO-O-TOLYLTHIOACETIC ACID [HSDB]
Acetic acid, 2-[(4-chloro-2-methylphenyl)thio]-
UNII-I66W18916F
ACETIC ACID,2-[(4-CHLORO-2-METHYLPHENYL)THIO]-
DTXSID1059109
SCHEMBL10778996
((4Chlorootolyl)thio)acetic acid
Acetic acid, ((4-chloro-o-tolyl)thio)-, (6CI,7CI,8CI)
GREQGIILILTWOH-UHFFFAOYSA-N
(4Chlorootolylmercapto)acetic acid
4Chloro2methylphenylthioglycolic acid
Acetic acid, ((4chlorootolyl)thio)
(4Chloro2methylbenzenemercapto)acetic acid
Acetic acid, ((4chloro2methylphenyl)thio)
Acetic acid, ((4-chloro-o-tolyl)thio)-,
Acetic acid, 2((4chloro2methylphenyl)thio)
NS00040417
2-(4-chloro-2-methyl-phenyl)sulfanylacetic acid
Q27280502
202-362-7