2033-27-4 Usage
Explanation
The compound's full name, indicating its structure and isomer.
Explanation
It belongs to a group of chemical compounds derived from dioxane.
Explanation
The compound appears as a colorless liquid at room temperature.
Explanation
It has a barely noticeable smell.
Explanation
It is mainly used as a solvent due to its ability to dissolve other substances.
Explanation
The compound has a specific arrangement of atoms, with the phenyl group and methyl group on the same side of the dioxane ring.
Explanation
The cisisomer of the compound has been identified as toxic, which means it can cause harm to living organisms.
Explanation
Exposure to the compound can lead to adverse effects on the respiratory system and central nervous system.
Explanation
Due to its toxicity, it is crucial to minimize exposure and potential harm to human health and the environment by adhering to safety guidelines.
Explanation
The compound may have negative effects on the environment if not handled and disposed of properly.
Classification
Dioxane derivative
Physical State
Colorless liquid
Odor
Faint
Primary Use
Solvent in industrial and manufacturing processes
Isomer
cis-
Toxicity
Known to be toxic
Health Risks
Respiratory system and central nervous system
Safety Precautions
Handle with caution and follow proper safety protocols
Environmental Impact
Potential harm to the environment
Check Digit Verification of cas no
The CAS Registry Mumber 2033-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2033-27:
(6*2)+(5*0)+(4*3)+(3*3)+(2*2)+(1*7)=44
44 % 10 = 4
So 2033-27-4 is a valid CAS Registry Number.
2033-27-4Relevant academic research and scientific papers
The Catalytic Asymmetric Intermolecular Prins Reaction
Diáz-Oviedo, C. David,Maji, Rajat,List, Benjamin
supporting information, p. 20598 - 20604 (2021/12/14)
Despite their significant potential, catalytic asymmetric reactions of olefins with formaldehyde are rare and metal-free approaches have not been previously disclosed. Here we describe an enantioselective intermolecular Prins reaction of styrenes and paraformaldehyde to form 1,3-dioxanes, using confined imino-imidodiphosphate (iIDP) Br?nsted acid catalysts. Isotope labeling experiments and computations suggest a concerted, highly asynchronous addition of an acid-activated formaldehyde oligomer to the olefin. The enantioenriched 1,3-dioxanes can be transformed into the corresponding optically active 1,3-diols, which are valuable synthetic building blocks.
