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4715-17-7

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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 this compound, 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.

4715-17-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-pentamethylene-4-methylene-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2-methylene-1,4-dioxa-spiro[4.5]decane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4715-17-7 SDS

4715-17-7Relevant articles and documents

METHOD FOR PRODUCING METHYLENE-1,3-DIOXOLANES

-

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.

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