6668-15-1 Usage
Description
[(Benzylsulfonyl)(chloro)methyl]benzene is a sulfonyl chloride chemical compound that features a benzene ring with both a benzylsulfonyl group and a chloromethyl group attached to it. [(benzylsulfonyl)(chloro)methyl]benzene is known for its utility in organic synthesis, particularly in the strategic introduction of the sulfonyl group into a variety of organic molecules. It is favored for its mild and selective nature as a source of sulfonyl chloride, which is often crucial in the synthesis of pharmaceuticals and other fine chemicals. Furthermore, its capacity to function as a mild electrophile renders it advantageous in the formation of carbon-carbon and carbon-heteroatom bonds within organic synthesis. However, due to its corrosive properties and potential hazards upon inhalation or ingestion, careful handling of this compound is paramount.
Uses
Used in Pharmaceutical Synthesis:
[(Benzylsulfonyl)(chloro)methyl]benzene is used as a reagent for the introduction of the sulfonyl group into organic molecules, which is particularly important in the synthesis of pharmaceuticals. Its mild and selective nature as a source of sulfonyl chloride makes it a valuable tool in the development of various medicinal compounds.
Used in Fine Chemicals Synthesis:
In the fine chemicals industry, [(benzylsulfonyl)(chloro)methyl]benzene is utilized as a reagent to introduce the sulfonyl group into target molecules. This is essential for the production of high-quality specialty chemicals that often have specific applications in various fields, such as agriculture, materials science, and the fragrance industry.
Used in Organic Synthesis for Bond Formation:
[(Benzylsulfonyl)(chloro)methyl]benzene is employed as a mild electrophile in organic synthesis, facilitating the construction of carbon-carbon and carbon-heteroatom bonds. This makes it a useful compound in the synthesis of complex organic molecules, which can be applied in a wide range of industries, including pharmaceuticals, materials science, and chemical research.
Used in Research and Development:
Due to its unique reactivity and selectivity, [(benzylsulfonyl)(chloro)methyl]benzene is also used in research and development settings. Chemists and scientists leverage this compound to explore new reaction pathways, develop innovative synthetic methods, and create novel molecular structures with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6668-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,6 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6668-15:
(6*6)+(5*6)+(4*6)+(3*8)+(2*1)+(1*5)=121
121 % 10 = 1
So 6668-15-1 is a valid CAS Registry Number.
