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Catalog Number:
23980
CAS Number:
1212087-13-2
Ácido S)-3-(4-Hidroxi-3-Nitrofenil)-2-(Fenilsulfonamido)Propanoico
Documents
$282.62 /100 mg
Tamaño
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Product Information

(S)-3-(4-Hydroxy-3-Nitrophenyl)-2-(Phenylsulfonamido)Propanoic Acid is a specialized compound with significant potential in pharmaceutical research and development. This compound, also known as (S)-2-(benzenesulfonamido)-3-(4-hydroxy-3-nitrophenyl)propanoic acid, features a unique structure that enhances its reactivity and interaction with biological systems. Its sulfonamide group contributes to its efficacy in various applications, particularly in the synthesis of bioactive molecules and as a potential lead compound in drug discovery.

Researchers have utilized this compound in studies focused on anti-inflammatory and analgesic properties, making it a valuable asset in the development of new therapeutic agents. Its ability to modulate biological pathways positions it as a promising candidate for further exploration in medicinal chemistry. The compound's distinctive characteristics, such as its selective interaction with specific enzymes, offer advantages over similar compounds, making it an attractive choice for professionals in the pharmaceutical industry seeking innovative solutions.

CAS Number
1212087-13-2
Molecular Formula
C15H14N2O7S
Molecular Weight
366.35
MDL Number
MFCD09998264
PubChem ID
75192758
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1212087-13-2
Molecular Formula
C15H14N2O7S
Molecular Weight
366.35
MDL Number
MFCD09998264
PubChem ID
75192758
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-3-(4-Hydroxy-3-Nitrophenyl)-2-(Phenylsulfonamido)Propanoic Acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting inflammatory diseases, due to its unique chemical structure that enhances bioactivity.
  • Biochemical Research: Researchers use it to study enzyme inhibition and protein interactions, providing insights into cellular processes and potential therapeutic targets.
  • Analytical Chemistry: It is employed as a standard in chromatographic methods, helping to ensure accuracy in the quantification of similar compounds in complex mixtures.
  • Material Science: The compound's properties make it suitable for developing new materials with specific functional characteristics, such as enhanced thermal stability and chemical resistance.
  • Environmental Studies: It is used in assessing the impact of pollutants, particularly in studies related to nitrophenol derivatives, aiding in the development of remediation strategies.

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