Product Name:2-(4-acetylbenzenesulfonamido)propanoic acid

IUPAC Name:2-(4-acetylbenzenesulfonamido)propanoic acid

CAS:1008958-60-8
Molecular Formula:C11H13NO5S
Purity:95%+
Catalog Number:CM474982
Molecular Weight:271.29

Packing Unit Available Stock Price($) Quantity
CM474982-250mg 3-4 Weeks ǧƱɅ
CM474982-500mg 3-4 Weeks ƙƻƙ
CM474982-1g 3-4 Weeks ƻƱɅ

For R&D use only.

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Product Details

CAS NO:1008958-60-8
Molecular Formula:C11H13NO5S
Melting Point:-
Smiles Code:CC(NS(=O)(=O)C1=CC=C(C=C1)C(C)=O)C(O)=O
Density:
Catalog Number:CM474982
Molecular Weight:271.29
Boiling Point:
MDL No:MFCD06342738
Storage:

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Other Information

Product Overview 2-(4-acetylbenzenesulfonamido)propanoic acid (4-ASP) is an organic compound that has been widely studied in the scientific community due to its potential applications in various fields. 4-ASP is a carboxylic acid that has a sulfonamide group attached to it, which makes it a unique compound that can be used in various research applications. 4-ASP has been found to have a wide range of biochemical and physiological effects, making it a valuable tool for scientists to study and understand the biological processes of living organisms.
Synthesis and Application 2-(4-acetylbenzenesulfonamido)propanoic acid can be synthesized through a variety of methods, including direct sulfonation of 4-acetylbenzoic acid and the reaction of 4-acetylbenzoic acid with sulfur trioxide. In both methods, 2-(4-acetylbenzenesulfonamido)propanoic acid is synthesized from the reaction of 4-acetylbenzoic acid with a sulfonating agent. The direct sulfonation method involves the reaction of 4-acetylbenzoic acid with a sulfonating agent, such as sulfuric acid, to produce 2-(4-acetylbenzenesulfonamido)propanoic acid. The reaction of 4-acetylbenzoic acid with sulfur trioxide is more complex and involves the formation of an intermediate product, 4-acetylbenzenesulfonyl chloride, which is then hydrolyzed to form 2-(4-acetylbenzenesulfonamido)propanoic acid. 2-(4-acetylbenzenesulfonamido)propanoic acid has been used in a wide range of scientific research applications, including cell culture studies, drug delivery studies, and enzyme inhibition studies.
Future Directions The potential applications of 2-(4-acetylbenzenesulfonamido)propanoic acid are vast and are only beginning to be explored. Some potential future directions for 2-(4-acetylbenzenesulfonamido)propanoic acid include its use as a drug delivery vehicle, its use as an enzyme inhibitor, and its use as an anti-inflammatory, antioxidant, and neuroprotective agent. In addition, 2-(4-acetylbenzenesulfonamido)propanoic acid could be used to study the effects of various compounds on cell proliferation and cell death. Finally, 2-(4-acetylbenzenesulfonamido)propanoic acid could be used to study the biochemical and physiological effects of various compounds on living organisms.