![3-(5-{[(3,4-Difluorophenyl)amino]carbonyl}-1,3,4-thiadiazol-2-yl)propanoic acid - chemical structure image](https://media.scbt.com/product/3-5--3-4-difluorophenyl-aminocarbonyl-1-3-4-thiadiazol-2-yl-propanoic-acid-structure_22_63_b_226370.jpg)
![3-(5-{[(3,4-Difluorophenyl)amino]carbonyl}-1,3,4-thiadiazol-2-yl)propanoic acid - chemical structure image](https://media.scbt.com/product/3-5--3-4-difluorophenyl-aminocarbonyl-1-3-4-thiadiazol-2-yl-propanoic-acid-structure_22_63_t_226370.jpg "Molecular structure of 3-(5-{[(3,4-Difluorophenyl)amino]carbonyl}-1,3,4-thiadiazol-2-yl)propanoic acid")
3-(5-{[(3,4-Difluorophenyl)amino]carbonyl}-1,3,4-thiadiazol-2-yl)propanoic acid
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N-Acetyl-S-(2-hydroxyethyl)-L-cysteine Dicyclohexylammonium Salt is a compound that functions as a reactive intermediate in organic synthesis. It acts as a nucleophile in various chemical reactions, particularly in the formation of carbon-carbon and carbon-sulfur bonds. N-Acetyl-S-(2-hydroxyethyl)-L-cysteine Dicyclohexylammonium Salt mechanism of action involves its ability to undergo nucleophilic substitution reactions, where the sulfur atom of the cysteine moiety attacks electrophilic carbon atoms in other molecules, leading to the formation of new chemical bonds. N-Acetyl-S-(2-Hydroxyethyl)-L-Cysteine Dicyclohexylammonium Salt is the synthesis of complex organic molecules and in the modification of biomolecules . Its reactivity and ability to participate in diverse chemical transformations make it a versatile for the development of novel compounds and materials in a laboratory setting.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-(5-{[(3,4-Difluorophenyl)amino]carbonyl}-1,3,4-thiadiazol-2-yl)propanoic acid, 500 mg | sc-309986 | 500 mg | $270.00 |