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Catalog Number:
05379
CAS Number:
129815-48-1
S-Acetylthioglycolic acid pentafluorophenyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
SAMA-OPfp, Pentafluorophenyl-S-acetylthioglycolate
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Product Information

S-Acetylthioglycolic acid pentafluorophenyl ester is a versatile compound known for its unique properties and applications in various fields, particularly in organic synthesis and pharmaceutical development. This ester is characterized by its pentafluorophenyl group, which enhances its reactivity and solubility, making it an excellent choice for researchers looking to develop new chemical entities. Its ability to act as a protecting group for thiols and its role in the synthesis of complex molecules highlight its significance in medicinal chemistry and material science.

In practical applications, S-Acetylthioglycolic acid pentafluorophenyl ester is utilized in the development of targeted drug delivery systems and as an intermediate in the synthesis of biologically active compounds. Its unique fluorinated structure provides advantages over similar compounds, such as improved stability and selectivity in reactions. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their products, making it a valuable addition to any chemical toolkit.

Synonyms
SAMA-OPfp, Pentafluorophenyl-S-acetylthioglycolate
CAS Number
129815-48-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H5O3F5S
Molecular Weight
300.1
MDL Number
MFCD00276401
PubChem ID
3569623
Appearance
White to off-white powder
Conditions
Store at ≤ - 15 °C
General Information
Synonyms
SAMA-OPfp, Pentafluorophenyl-S-acetylthioglycolate
CAS Number
129815-48-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H5O3F5S
Molecular Weight
300.1
MDL Number
MFCD00276401
PubChem ID
3569623
Appearance
White to off-white powder
Conditions
Store at ≤ - 15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

S-Acetylthioglycolic acid pentafluorophenyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in creating drugs that target specific biological pathways.
  • Bioconjugation: Its unique structure allows for effective bioconjugation processes, making it valuable in developing targeted drug delivery systems and diagnostic agents.
  • Analytical Chemistry: Used as a reagent in analytical methods, it helps in the detection and quantification of thiol-containing compounds, which are crucial in many biochemical assays.
  • Material Science: This ester is applied in the formulation of advanced materials, enhancing properties such as durability and chemical resistance in coatings and polymers.
  • Environmental Applications: It plays a role in environmental chemistry, particularly in the remediation of contaminated sites by facilitating the breakdown of hazardous substances.

Citations