Nombre del producto:2,6-Dichlorobenzene-1-sulfonyl chloride

IUPAC Name:2,6-dichlorobenzene-1-sulfonyl chloride

CAS:6579-54-0
Fórmula molecular:C6H3Cl3O2S
Pureza:95%
Número de catálogo:CM254370
Peso molecular:245.5

Unidad de embalaje Stock disponible Precio($) Cantidad
CM254370-25g in stock ƱǕ

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :6579-54-0
Fórmula molecular:C6H3Cl3O2S
Punto de fusión:-
Código de sonrisas:O=S(C1=C(Cl)C=CC=C1Cl)(Cl)=O
Densidad:
Número de catálogo:CM254370
Peso molecular:245.5
Punto de ebullición:
Nº Mdl:MFCD00052311
Almacenamiento:Keep in inert atmosphere, store at 2-8°C.

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.

Column Infos

Related Products



Product Other Information

Product Overview 2,6-Dichlorobenzenesulfonyl chloride (DCBS) is a chemical compound that has been used in a variety of scientific research applications due to its unique properties and structure.
Synthesis Method 2,6-Dichlorobenzenesulfonyl chloride can be synthesized through a variety of methods, including the direct reaction of 2,6-dichlorobenzene with sulfur dichloride or by the reaction of 2,6-dichlorobenzene with thionyl chloride. The direct reaction of 2,6-dichlorobenzene with sulfur dichloride is the most common method for synthesizing 2,6-Dichlorobenzenesulfonyl chloride.
Chemical Properties The advantages of using 2,6-Dichlorobenzenesulfonyl chloride in lab experiments include its low toxicity and its ability to react with a variety of nucleophiles. Additionally, 2,6-Dichlorobenzenesulfonyl chloride is relatively inexpensive and easy to obtain. 
Synthesis and Application It has been used in the synthesis of peptides and peptidomimetics, as well as in the synthesis of other peptide-based molecules. Additionally, 2,6-Dichlorobenzenesulfonyl chloride has been used in the synthesis of a variety of pharmaceuticals, dyes, and agrochemicals.
Future Directions These include its potential use in the synthesis of peptide-based drugs, its potential use in the synthesis of agrochemicals, and its potential use in the synthesis of dyes. Additionally, further research is needed to understand the biochemical and physiological effects of 2,6-Dichlorobenzenesulfonyl chloride and to develop new methods for its synthesis.