4715-17-7 Usage
Chemical Structure
Cyclic ether with a spiro ring system
Explanation
The compound is a cyclic ether, meaning it contains an oxygen atom connected to two carbon atoms in a ring structure. The spiro ring system refers to the presence of two rings connected by a single carbon atom.
Explanation
A methylene group (-CH2-) is a two-carbon fragment with a single bond between the carbons and a hydrogen atom attached to one of the carbons. In 1,4-Dioxaspiro[4.5]decane, 2-methylene-, the methylene group is connected to the spiro carbon atom.
Explanation
The compound is used as a starting material or intermediate in the synthesis of various organic compounds, including those used in the pharmaceutical and fine chemical industries.
Explanation
The compound serves as a reagent, which is a substance used to initiate or facilitate a chemical reaction. In this case, it is particularly useful in the synthesis of heterocyclic compounds, which are organic compounds containing a ring of atoms with at least one non-carbon atom.
Explanation
Due to its unique spiro structure, the compound has potential applications in the development of new materials and polymers, which are large molecules composed of repeating structural units.
Explanation
The compound is soluble in organic solvents, such as alcohols, ethers, and hydrocarbons, which allows for its use in various chemical reactions and processes.
Explanation
The compound is relatively stable under normal conditions, meaning it does not readily undergo decomposition or react with other substances. This stability is important for its use in organic synthesis and as a building block for other compounds.
Methylene Group
Attached to the spiro carbon atom
Application
Organic synthesis and building block for pharmaceuticals and fine chemicals
Use as a Reagent
In the formation of heterocyclic compounds
Potential Applications
Development of new materials and polymers
Solubility
Soluble in organic solvents
Stability
Relatively stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 4715-17-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4715-17:
(6*4)+(5*7)+(4*1)+(3*5)+(2*1)+(1*7)=87
87 % 10 = 7
So 4715-17-7 is a valid CAS Registry Number.
4715-17-7Relevant academic research and scientific papers
METHOD FOR PRODUCING METHYLENE-1,3-DIOXOLANES
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Paragraph 0051; 0052; 0053; 0054; 0056; 0057; 0058; 0059, (2015/01/07)
The present invention relates to a novel method for preparing methylene-1,3-dioxolanes of the general formula (1) in which R1 and R2 have the meanings stated in the description. Methylene-1,3-dioxolanes are important intermediates for preparing pyrazoles and anthranilic acid amides, which may be used as insecticides.
TETRAFLUOROBORIC ACID - A NEW CATALYST FOR THE SYNTHESIS OF 1,3-DIOXOLANES. PREPARATION OF HYDROXYACETONE
Gevorkyan, A. A.,Kazaryan, P. I.,Avakyan, O. V.,Vardanyan, R. A.
, p. 27 - 30 (2007/10/02)
It is established that tetrafluoroboric acid (HBF4) is an effective catalyst for halogen substitution reactions of oxiranes (epichlorohydrin and 1-bromo-3-methyl-2,3-epoxybutane) with aldehydes and ketones, forming 1,3-dioxolanes in high yield.
RADICAL THIYLATION OF SOME UNSATURATED 1,3-DIOXOLANES
Etlis, V. S.,Shomina, F. N.,Tsareva, L. A.,Semenova, E. A.,Degtyareva, L. M.
, p. 1978 - 1982 (2007/10/02)
The radical addition of thiols to unsaturated 1,3-dioxolanes leads to the formation of the products from addition against the Markovnikov rule.Identical thioethers are produced as a result of nucleophilic substitution of the corresponding chloromethyl derivatives of 1,3-dioxolanes by sodium butanethiolate or phenylmethanethiolate.
