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Fenclonine

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Identification
Molecular formula
C8H7ClO2S
CAS number
7424-00-2
IUPAC name
2-(2-chlorophenyl)sulfanylacetic acid
State
State

At room temperature, Fenclonine is in a solid state, commonly appearing as a white crystalline powder.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
335.10
Boiling point (Kelvin)
608.25
General information
Molecular weight
202.66g/mol
Molar mass
202.6600g/mol
Density
1.5140g/cm3
Appearence

Fenclonine is typically a crystalline solid. Its specific characteristics can vary slightly depending on the conditions, but it is generally found as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(2-chlorophenyl)sulfanylacetic acid

The solubility of 2-(2-chlorophenyl)sulfanylacetic acid presents interesting characteristics worth exploring. This compound, with the formula C9H8ClO2S, is known to demonstrate moderate solubility in various solvents, which can be attributed to its unique structural features.

Factors Influencing Solubility

Several factors play a significant role in determining the solubility of this compound:

  • Polarity: The presence of the carboxylic acid group (-COOH) allows for hydrogen bonding, enhancing its solubility in polar solvents like water.
  • Chlorine Substitution: The electronegative chlorine atom attached to the aromatic ring influences the overall polarity, which can affect solubility in organic solvents.
  • Hydrophobic Interactions: The aromatic portion of the molecule can lead to decreased solubility in highly polar environments but may increase solubility in less polar organic solvents.

General Observations

In general, one can expect:

  • Moderate solubility in polar solvents such as water and alcohols.
  • Increased solubility in non-polar solvents like dichloromethane or chloroform due to hydrophobic interactions.

Understanding the solubility of 2-(2-chlorophenyl)sulfanylacetic acid is essential for applications in pharmaceutical contexts, where the solubility can directly influence bioavailability and efficacy.

Interesting facts

Exploring 2-(2-chlorophenyl)sulfanylacetic Acid

2-(2-chlorophenyl)sulfanylacetic acid, often abbreviated as CPAA, is a fascinating compound that has captured the attention of chemists due to its unique structure and potential applications. Below are some insightful facts about this intriguing chemical:

  • Functional Groups: The presence of both a sulfanic group and a carboxylic acid in CPAA makes it an excellent subject for studying the reactivity and properties of multifunctional molecules.
  • Biological Significance: This compound has shown promise in various biological studies, including potential anti-inflammatory and analgesic effects, making it a candidate for pharmaceutical research.
  • Reactivity: The aromatic ring (2-chlorophenyl) enhances the electrophilicity of the sulfur atom, leading to interesting reactions, especially in the presence of nucleophiles.
  • Synthesis Potential: The synthesis of CPAA can be achieved through various pathways, including the nucleophilic substitution reaction, providing valuable insights into synthetic organic chemistry techniques.

As aptly noted in the field, “Chemical research is not only about the compounds we study but also about the connections they help us forge in our understanding of nature.” The exploration of CPAA exemplifies how every compound can unlock new doors in the vast world of chemistry.

In conclusion, 2-(2-chlorophenyl)sulfanylacetic acid is more than just a chemical formula; it serves as a bridge between complex organic structures and potential real-world applications, making it a vital compound for chemists to investigate further.

Synonyms
18619-18-6
O-CHLOROPHENYL THIOACETIC ACID
[(2-chlorophenyl)thio]acetic acid
o-Chlorophenylmercaptoacetic acid
UNII-LFQ8288EHB
LFQ8288EHB
Acetic acid, ((o-chlorophenyl)thio)-
Acetic acid, ((2-chlorophenyl)thio)-
HSDB 2670
NSC 513490
NSC-513490
DTXSID80171863
Acetic acid, [(o-chlorophenyl)thio]-
Acetic acid, [(2-chlorophenyl)thio]-
((2-CHLOROPHENYL)THIO)ACETIC ACID
(2-CHLOROPHENYLSULFANYL)ACETIC ACID
ACETIC ACID, 2-((2-CHLOROPHENYL)THIO)-
Acetic acid, 2-[(2-chlorophenyl)thio]-
oChlorophenyl thioacetate
oChlorophenylmercaptoacetic acid
DTXCID6094354
Acetic acid, ((ochlorophenyl)thio)
Acetic acid, ((2chlorophenyl)thio)
Acetic acid, ((o-chlorophenyl)thio)-(8CI)
Acetic acid, ((2-chlorophenyl)thio)-(9CI)
o-Chlorophenyl thioacetate
2-((2-Chlorophenyl)thio)acetic acid
2-(2-chlorophenyl)sulfanylacetic acid
o-chlorophenylthioacetate
MFCD01910097
2-[(2-chlorophenyl)sulfanyl]acetic acid
2-[(2-Chlorophenyl)thio]acetic Acid
SCHEMBL1157659
SCHEMBL29812491
DRTNNSJQBCUQML-UHFFFAOYSA-N
HMS1788P01
CS-B1577
TAA61918
2-((2-Chlorophenyl)thio)aceticacid
NSC513490
(2-Chloro-phenylsulfanyl)-acetic acid
AKOS000117531
acetic acid, 2-(2-chlorophenyl)thio-
O-CHLOROPHENYL THIOACETATE [HSDB]
CS-16918
SY133145
EN300-07701
C13412
Q27282957
Z55903470