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AB50085

1072-53-3 | Ethylenesulfate

Packsize Purity Availability Price Discounted Price    Quantity
5g 98% in stock $5.00 $4.00 -   +
10g 98% in stock $6.00 $5.00 -   +
25g 98% in stock $8.00 $6.00 -   +
100g 98% in stock $18.00 $13.00 -   +
500g 98% in stock $71.00 $50.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB50085
Chemical Name: Ethylenesulfate
CAS Number: 1072-53-3
Molecular Formula: C2H4O4S
Molecular Weight: 124.1158
MDL Number: MFCD00221769
SMILES: O=S1(=O)OCCO1
NSC Number: 526594

 

Computed Properties
Complexity: 128  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 4  
XLogP3: -0.5  

 

 

Upstream Synthesis Route
  • 1,3,2-Dioxathiolane 2,2-dioxide, often referred to simply as dioxathiolane dioxide, is a versatile compound that finds a wide range of applications in chemical synthesis. It is commonly used as a powerful oxidizing agent in organic chemistry reactions. This compound's unique structure allows it to facilitate various oxidation processes efficiently and selectively, making it a valuable tool for synthetic chemists.In chemical synthesis, 1,3,2-Dioxathiolane 2,2-dioxide is frequently employed in oxidation reactions to convert primary and secondary alcohols into their corresponding aldehydes and ketones, respectively. This process is essential in the production of various organic compounds, including pharmaceuticals, fragrances, and fine chemicals. Additionally, dioxathiolane dioxide can also be utilized in the oxidation of sulfides to sulfoxides and sulfones, showcasing its versatility in synthetic applications.Furthermore, this compound's high reactivity and selectivity make it a preferred reagent in complex synthesis pathways where precise control over functional group transformations is crucial. Its compatibility with a wide range of functional groups and its ability to operate under mild reaction conditions further contribute to its popularity in organic synthesis.Overall, 1,3,2-Dioxathiolane 2,2-dioxide plays a vital role in chemical synthesis by enabling efficient and selective oxidation reactions, making it a valuable asset for chemists working in various fields of organic chemistry.
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