2986-72-3 Usage
Description
(Allyloxy)cyclododecane, with the molecular formula C18H34O and a molecular weight of 282.46 g/mol, is an allyl ether derivative of cyclododecane, a cyclic hydrocarbon with 12 carbon atoms and a high melting point. This chemical compound is known for its pleasant odor and taste, making it a valuable component in various industries.
Uses
Used in Fragrance and Flavor Industry:
(Allyloxy)cyclododecane is used as a fragrance and flavoring agent for its appealing scent and taste, enhancing the sensory experience of various consumer products.
Used in Polymer Production:
(Allyloxy)cyclododecane serves as a crucial ingredient in the production of polymers, contributing to the development of new materials with specific properties and applications.
Used as a Solvent in Industrial Processes:
(Allyloxy)cyclododecane is utilized as a solvent in certain industrial processes, where its chemical properties facilitate specific reactions or help dissolve other substances.
Used in Organic Chemistry for Synthesis:
It has been studied for its potential as a building block in the synthesis of novel materials and compounds, expanding the horizons of organic chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 2986-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2986-72:
(6*2)+(5*9)+(4*8)+(3*6)+(2*7)+(1*2)=123
123 % 10 = 3
So 2986-72-3 is a valid CAS Registry Number.
2986-72-3Relevant articles and documents
Reliably Regioselective Dialkyl Ether Cleavage with Mixed Boron Trihalides
Atienza, Bren Jordan P.,Truong, Nam,Williams, Florence J.
supporting information, p. 6332 - 6335 (2018/10/09)
A protocol for the regioselective cleavage of unsymmetrical alkyl ethers to generate alkyl alcohol and alkyl bromide products is described. A mixture of trihaloboranes triggers this conversion and exhibits improved reactivity profiles (regioselectivity and yield) compared with BBr3 alone. Additionally, this procedure allows the efficient synthesis of (B-Cl) dialkyl boronate esters. There are limited methods to generate acyclic dialkoxyboryl chlorides, and these intermediates constitute important synthons in main-group chemistry.
