16486-85-4 Usage
Synonyms
1,3-Dioxolane, hexenyl (8CI,9CI)
Explanation
Synonyms are alternative names for a chemical compound. In this case, the compound is also known as 1,3-Dioxolane, hexenyl.
Explanation
A dioxolane derivative is an organic compound containing a five-membered ring with two oxygen atoms. 1,3-Dioxolane, 2-(1-hexenyl)- (8CI,9CI) is a derivative of dioxolane.
Explanation
The 1-hexenyl group is an unsaturated hydrocarbon, which means it contains carbon-carbon double bonds. In 1,3-Dioxolane, 2-(1-hexenyl)- (8CI,9CI), the 1-hexenyl group is attached to the dioxolane ring.
Explanation
This chemical compound may be used as a starting material or intermediate in the production of other organic compounds, making it valuable in various industrial processes.
Explanation
Due to its chemical properties, it is essential to handle 1,3-Dioxolane, 2-(1-hexenyl)- (8CI,9CI) carefully and follow safety guidelines to minimize potential risks associated with its use or mishandling.
Explanation
The structure of 1,3-Dioxolane, 2-(1-hexenyl)- (8CI,9CI) consists of a dioxolane ring (a five-membered ring with two oxygen atoms) and a 1-hexenyl group (an unsaturated hydrocarbon) attached to it.
Type of Compound
Dioxolane derivative
Unsaturated Hydrocarbon
1-Hexenyl group attached
Industrial Applications
Precursor in the synthesis of other organic compounds
Safety Precautions
Handle with caution and follow proper safety protocols
Chemical Structure
Five-membered ring with two oxygen atoms and a 1-hexenyl group
Check Digit Verification of cas no
The CAS Registry Mumber 16486-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16486-85:
(7*1)+(6*6)+(5*4)+(4*8)+(3*6)+(2*8)+(1*5)=134
134 % 10 = 4
So 16486-85-4 is a valid CAS Registry Number.
16486-85-4Relevant academic research and scientific papers
Oxidative cyclization reactions: Controlling the course of a radical cation-derived reaction with the use of a second nucleophile
Redden, Alison,Perkins, Robert J.,Moeller, Kevin D.
supporting information, p. 12865 - 12868 (2014/01/06)
Construction of new ring systems: Oxidative cyclizations (see picture; RVC=reticulated vitreous carbon) have been conducted that use two separate intramolecular nucleophiles to trap an enol ether-derived radical cation intermediate. The reactions provide
