AA01399
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $191.00 | $134.00 | - + | |
250mg | 95% | in stock | $326.00 | $228.00 | - + | |
1g | 95% | in stock | $880.00 | $616.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA01399 |
Chemical Name: | Disulfide, bis(2-chloroethyl) |
CAS Number: | 1002-41-1 |
Molecular Formula: | C4H8Cl2S2 |
Molecular Weight: | 191.1423 |
MDL Number: | MFCD20621166 |
SMILES: | ClCCSSCCCl |
1,2-Bis(2-chloroethyl)disulfane, also known as a sulfur mustard analog, is a key compound used in chemical synthesis for its versatile applications in organic chemistry. This compound is commonly utilized as a reactive agent in the creation of various sulfur-containing compounds, including thioethers and disulfides. Its unique structure, featuring two chloroethyl groups attached to a disulfane backbone, allows for effective crosslinking reactions and the formation of complex molecular structures.In chemical synthesis, 1,2-Bis(2-chloroethyl)disulfane serves as a valuable building block for the construction of biologically active molecules, pharmaceutical intermediates, and materials with specialized properties. Its ability to participate in nucleophilic substitution reactions and undergo oxidative transformations makes it an indispensable reagent for the preparation of sulfur-rich compounds with diverse applications in drug discovery, materials science, and bioconjugation chemistry.Furthermore, the reactivity of 1,2-Bis(2-chloroethyl)disulfane can be harnessed for the modification of biomolecules, such as proteins and peptides, through selective sulfhydryl crosslinking and conjugation strategies. This compound offers researchers a powerful tool for the site-specific functionalization of target molecules, enabling the design of novel bioconjugates and engineered materials with tailored properties.Overall, the use of 1,2-Bis(2-chloroethyl)disulfane in chemical synthesis demonstrates its significance in enabling the construction of intricate molecular architectures and the development of innovative compounds with potential applications across various fields of science and technology.