6413-31-6 Usage
Heterocyclic organic compound
The compound contains both furan and dioxane rings, which are heterocyclic, meaning they consist of more than one type of atom in the ring structure.
Furan ring
A five-membered ring with one oxygen atom and four carbon atoms, contributing to the compound's heterocyclic nature.
Dioxane ring
A six-membered ring with two oxygen atoms and four carbon atoms, also contributing to the compound's heterocyclic nature.
Organic synthesis
2-(furan-2-yl)-4-methyl-1,3-dioxane is commonly used as an intermediate in organic synthesis, which is the process of creating new compounds from simpler molecules.
Building block in pharmaceuticals, agrochemicals, and fine chemicals
The compound serves as a starting material or precursor in the production of various pharmaceuticals, agrochemicals (chemicals used in agriculture), and fine chemicals (high-value, specialized chemicals).
Potential use in drug delivery systems
Researchers have studied 2-(furan-2-yl)-4-methyl-1,3-dioxane as a possible component in drug delivery systems, which are designed to transport and release drugs in a controlled manner.
Check Digit Verification of cas no
The CAS Registry Mumber 6413-31-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6413-31:
(6*6)+(5*4)+(4*1)+(3*3)+(2*3)+(1*1)=76
76 % 10 = 6
So 6413-31-6 is a valid CAS Registry Number.
6413-31-6Relevant articles and documents
Synthesis and structure analysis of cyclic furfural acetals
Melnitskaya,Kuramshin,Khlebnikova,Melnitskii,Kantor
, p. 908 - 914 (2007/10/03)
Quantum chemical calculations and the PMR method are used to show that the preferable conformation of cyclic furfural acetals is a chair with an axial orientation of the furyl substituent. In 2-(furyl-2′)-5-ethyl-5-oxymethyl-1,3-dioxane, the conformation equilibrium is shifted toward the trans-isomer with diaxial positions of the furyl and oxymethyl groups. The results of calculations suggest that the synthesis can lead to a cis-isomer with an axial orientation of the furyl and equatorial oxymethyl groups. It was shown experimentally that the synthesis leads to a mixture of trans- and cis-isomers. Mild conditions (room temperature, aqueous medium) lead to formation of the trans-isomer and small amounts of the cis-isomer (less than 2%). In rigid conditions (boiling in aromatic hydrocarbons), up to 20% of the cis-isomer is formed. 1998 Plenum Publishing Corporation.
