343864-66-4 Usage
Explanation
The compound's full chemical name, which includes its functional groups and substituents.
Explanation
An alternative name for the compound, which highlights its core structure and substituents.
Explanation
The compound belongs to the class of organic compounds, which are primarily composed of carbon and hydrogen atoms.
Explanation
The compound is a colorless liquid that evaporates easily at room temperature.
Explanation
The compound has a noticeable and potent odor.
Explanation
The compound is commonly used in the synthesis of various organic compounds, making it valuable in the chemical industry.
Explanation
The compound can react with oxidizing agents, which may lead to combustion or the formation of explosive peroxides.
Explanation
Due to its reactivity, it is essential to handle and store the compound carefully to prevent accidents or hazardous situations.
Explanation
The compound's reactivity with oxidizing agents can result in hazardous reactions, such as combustion or the formation of explosive peroxides.
Category
Organic Compounds
Physical State
Colorless and Volatile Liquid
Odor
Strong
Industrial Applications
Organic Synthesis
Reactivity
Potential to React with Oxidizing Agents
Safety Precautions
Handle and Store with Caution
Hazardous Reactions
Combustion and Formation of Explosive Peroxides
Check Digit Verification of cas no
The CAS Registry Mumber 343864-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,8,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 343864-66:
(8*3)+(7*4)+(6*3)+(5*8)+(4*6)+(3*4)+(2*6)+(1*6)=164
164 % 10 = 4
So 343864-66-4 is a valid CAS Registry Number.
343864-66-4Relevant academic research and scientific papers
Nickel-Catalyzed Asymmetric Kumada Cross-Coupling of Symmetric Cyclic Sulfates
Eno, Meredith S.,Lu, Alexander,Morken, James P.
supporting information, p. 7824 - 7827 (2016/07/11)
Nickel-catalyzed enantioselective cross-couplings between symmetric cyclic sulfates and aromatic Grignard reagents are described. These reactions are effective with a broad range of substituted cyclic sulfates and deliver products with asymmetric tertiary carbon centers. Mechanistic experiments point to a stereoinvertive SN2-like oxidative addition of a nickel complex to the electrophilic substrate.
2-Oxo-1,3,2-dioxathianes. I. Preparation of the Alkyl-substituted Derivatives
Virtanen, Terttu,Nikander, Hannu
, p. 113 - 116 (2007/10/02)
2-Oxo-1,3,2-dioxathiane, all methyl- and several other alkyl-substituted 2-oxo-1,3,2-dioxathianes have been synthesized by condensing 1,3-alkanediols and thionyl chloride.The amount of the S==O-axial and S==O-equatorial isomers can be controlled by adding pyridine to the reaction mixture.
