Product Name:5,6-Dimethylpyridine-3-sulfonyl chloride

IUPAC Name:5,6-dimethylpyridine-3-sulfonyl chloride

CAS:1781875-71-5
Molecular Formula:C7H8ClNO2S
Purity:95%+
Catalog Number:CM631237
Molecular Weight:205.66

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Product Details

CAS NO:1781875-71-5
Molecular Formula:C7H8ClNO2S
Melting Point:-
Smiles Code:CC1=C(C)N=CC(=C1)S(Cl)(=O)=O
Density:
Catalog Number:CM631237
Molecular Weight:205.66
Boiling Point:
MDL No:
Storage:

Category Infos

Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

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Product Overview 5,6-Dimethylpyridine-3-sulfonyl chloride (DMSC) is a sulfonyl chloride derivative of 5,6-dimethylpyridine, a heterocyclic aromatic compound. DMSC is a versatile reagent used in organic synthesis, particularly for the preparation of sulfonamides, sulfonamides, and sulfones.
Synthesis Method 5,6-Dimethylpyridine-3-sulfonyl chloride can be synthesized from 5,6-dimethylpyridine and chlorosulfonic acid. The reaction of 5,6-dimethylpyridine with chlorosulfonic acid yields the corresponding sulfonyl chloride, which is then purified by column chromatography. 
Chemical Properties 5,6-Dimethylpyridine-3-sulfonyl chloride has the main advantage of using in laboratory experiments is its ability to act as a polar aprotic solvent, which makes it an ideal reagent for a variety of organic reactions. Additionally, 5,6-Dimethylpyridine-3-sulfonyl chloride is a relatively inexpensive reagent. 5,6-Dimethylpyridine-3-sulfonyl chloride is a strong nucleophilic reagent, which means that it can react with a variety of electrophilic substrates. This can lead to unwanted side reactions, which can limit the usefulness of 5,6-Dimethylpyridine-3-sulfonyl chloride in certain experiments.
Synthesis and Application 5,6-Dimethylpyridine-3-sulfonyl chloride has been used as a reagent in a variety of organic synthesis reactions, including the synthesis of sulfonamides, sulfonamides, and sulfones. It has also been used in the synthesis of heterocyclic compounds, such as pyridines and thiophenes. 5,6-Dimethylpyridine-3-sulfonyl chloride has also been used in the synthesis of peptides and amino acids, as well as in the synthesis of polymers and other materials.
Future Directions Some of the future directions for 5,6-Dimethylpyridine-3-sulfonyl chloride include the development of new synthesis methods, the investigation of its biochemical and physiological effects, and the exploration of its potential applications in drug design and delivery. Additionally, further research is needed to explore the potential of 5,6-Dimethylpyridine-3-sulfonyl chloride as a catalyst in a variety of organic reactions. Finally, further research is needed to explore the potential of 5,6-Dimethylpyridine-3-sulfonyl chloride as a reagent for the synthesis of heterocyclic compounds, peptides, and amino acids.