4705-18-4

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Heterocyclic organic compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, hydrogen, oxygen, and sulfur.
3. Contains sulfur and oxygen atoms

Explanation

The compound's structure includes sulfur and oxygen atoms, which contribute to its unique chemical properties.
4. Used in synthesis of pharmaceuticals and agrochemicals

Explanation

The compound serves as a starting material or intermediate in the production of various drugs and chemicals used in agriculture.
5. Building block for other organic compounds

Explanation

It can be used to create a variety of other organic molecules, making it a versatile component in chemical synthesis.
6. Applications in medicinal chemistry and drug development

Explanation

Due to its chemical properties, the compound has potential uses in creating new medicines and therapies.
7. Potential health risks and environmental hazards

Explanation

The compound may pose risks to human health and the environment if not handled, used, and disposed of properly.
8. Caution required in handling

Explanation

Special care should be taken when working with 1,3,2-Benzodioxathiole, hexahydro-, 2-oxide to minimize the risk of exposure and potential harm.

Upstream product

• 1792-81-0 cis-1,2-cyclohexane 
• 1460-57-7 trans-1,2-cyclohexandiol 
• 286-20-4 cyclohexane-1,2-epoxide 
• 931-17-9 1,2-Cyclohexanediol 

Downstream Products

• 6970-90-7 cis-hexahydro-benz-[1,3,2]-dioxathiolane-2,2-dioxide 
• 108-94-1 cyclohexanone 
• 1792-81-0 cis-1,2-cyclohexane 
• 110357-47-6 cis-Cyclohexandiol-(1,2)-monosulfat 
• 4705-17-3 trans-Cyclohexandiol-(1,2)-sulfat 

Relevant academic research and scientific papers

Aluminum-Catalyzed Formation of Functional 1,3,2-Dioxathiolane 2-Oxides from Sulfur Dioxide: An Easy Entry towards N-Substituted Aziridines

Aluminum(III) complexes derived from aminotriphenolate ligands are shown to be excellent catalysts for the formation of cyclic sulfites from a range of (functionalized) terminal and internal epoxides, and ex situ generated sulfur dioxide. The developed catalytic protocol is characterized by its operational simplicity, wide scope in epoxide reaction partners, good to excellent isolated yields and mild reaction conditions [50–70 °C, p(SO2) a three-step protocol. (Figure presented.).

Guanidine functionalized ionic liquid and preparation method and application thereof

The present invention discloses a functionalized ionic liquid of guanidine and preparation method and application thereof, the cation of the ionic liquid is 1,1,3,3-tetramethylguanidine cation, the anion is methoxyacetic acid anion or ethoxyacetic acid an

Process for Preparing Optically Active Diphosphanes

The present invention relates to a process for preparing optically active bisphosphinylalkanes from the correspondingly substituted, racemic 1,2-diols. The optically active bisphosphinylalkanes which can be obtained in this way are suitable as ligands for preparing chiral transition metal catalysts.

Reaction of diethylaminosulfur trifluoride with diols

Diethylaminosulfur trifluoride (DAST) reacts with dialcohols to give difluorides, sulfite esters or cyclic ethers depending on the number of carbons separating the two alcohol groups.Vicinal and 1,3-diols give large amounts of sulfite ester products while butane-1,4-diol gives almost exclusively the cyclic ether tetrahydrofuran.Terminal dialcohols longer than four carbons give primarily difluoride products.Semiempirical calculations indicate a preference for cyclic intermediates when four or less carbons separate the two alcohol moieties.These cyclic intermediates lead directly to the cyclic ethers and sulfite ester products.