Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
19071
CAS Number:
361336-73-4
Ester méthylique de l'acide 5-amino-2-phénylsulfanyl-benzoïque
Purity:
≥ 95 % (dosage)
Synonym(s):
5-amino-2-(phénylthio)benzoate de méthyle
Documents
$65.40 /250 mg
Taille
Request Bulk Quote
Product Information

5-Amino-2-phenylsulfanyl-benzoic acid methyl ester is a versatile compound known for its significant applications in pharmaceutical and chemical research. This compound features a unique structure that includes an amino group and a phenylsulfanyl moiety, making it an attractive candidate for the synthesis of various bioactive molecules. Researchers often utilize this compound in the development of novel drugs, particularly in the fields of anti-inflammatory and antimicrobial agents. Its ability to act as a building block in organic synthesis allows for the creation of complex structures that can lead to innovative therapeutic solutions.

In addition to its pharmaceutical relevance, 5-Amino-2-phenylsulfanyl-benzoic acid methyl ester is also employed in materials science for the development of functionalized polymers and coatings. Its unique chemical properties enable enhanced performance characteristics, such as improved stability and reactivity in various applications. This compound stands out among similar products due to its multifunctionality and the potential for diverse applications across multiple industries, making it a valuable addition to any research or production portfolio.

Synonyms
5-amino-2-(phénylthio)benzoate de méthyle
CAS Number
361336-73-4
Purity
≥ 95 % (dosage)
Molecular Formula
C 14 H 13 NO 2 S
Molecular Weight
259.33
MDL Number
MFCD06658472
PubChem ID
11821319
Appearance
Liquide orange
Conditions
Conserver à 0-8 °C
General Information
Synonyms
5-amino-2-(phénylthio)benzoate de méthyle
CAS Number
361336-73-4
Purity
≥ 95 % (dosage)
Molecular Formula
C 14 H 13 NO 2 S
Molecular Weight
259.33
MDL Number
MFCD06658472
PubChem ID
11821319
Appearance
Liquide orange
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Amino-2-phenylsulfanyl-benzoic acid methyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting inflammatory diseases due to its unique functional groups.
  • Biochemical Research: It is used in studies exploring enzyme inhibition and protein interactions, helping researchers understand biological pathways and develop new therapeutic strategies.
  • Material Science: The compound finds applications in creating novel materials with specific electronic properties, making it valuable in the development of sensors and conductive polymers.
  • Organic Synthesis: As a versatile building block, it facilitates the creation of more complex organic molecules, aiding chemists in designing new compounds for various applications.
  • Analytical Chemistry: It is employed in the development of analytical methods for detecting and quantifying other compounds, enhancing the accuracy of chemical analysis in laboratories.

Citations