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1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether . The compound is often called simply dioxane because the other dioxane isomers ( 1,2- and 1,3- ) are rarely encountered.
1,3-Dioxane or m-dioxane is an organic compound with the molecular formula (CH 2) 4 O 2. It is a saturated six-membered heterocycle with two oxygen atoms in place of carbon atoms at the 1- and 3- positions. 1,4-Dioxane, which is of greater commercial value, is an isomer. Both dioxanes are colorless liquids. [1]
Germanium dichloride dioxane is a chemical compound with the formula GeCl 2 (C 4 H 8 O 2), where C 4 H 8 O 2 is 1,4-dioxane. It is a white solid. The compound is notable as a source of Ge(II), which contrasts with the pervasiveness of Ge(IV) compounds. This dioxane complex represents a well-behaved form of germanium dichloride.
Dioxane may refer to the following chemical compounds: 1,2-dioxane; 1,3-dioxane; 1,4-dioxane This page was last edited on 13 October 2023, at 00:57 (UTC). Text is ...
The structure of gas-phase molecular GeCl 2 shows that it is a bent molecule, as predicted by VSEPR theory. [5] The dioxane complex, GeCl 2 ·dioxane, has been used as a source of molecular GeCl 2 for reaction syntheses, as has the in situ reaction of GeCl 4 and Ge metal. GeCl 2 is quite reactive and inserts into many types of chemical bonds. [6]
The resulting hydroquinone is poorly soluble in typical reaction solvents (dioxane, benzene, alkanes), which facilitates workup. Solutions of DDQ in benzene are red, due to the formation of a charge-transfer complex. [9]
The benzodioxans are a group of isomeric chemical compounds with the molecular formula C 8 H 8 O 2. [1] There are three isomers of benzodioxan, as the second atom of oxygen of the dioxane can be in a second, third or fourth position: 1,2-dioxane, 1,3-dioxane and 1,4-dioxane, which respectively give 1,2-benzodioxan, 1,3-benzodioxan and 1,4-benzodioxan.
Neosporol is a natural product that includes a 1,3-dioxolane moiety, and is an isomer of sporol which has a 1,3-dioxane ring. [9] The total synthesis of both compounds has been reported, and each includes a step in which a dioxolane system is formed using trifluoroperacetic acid (TFPAA), prepared by the hydrogen peroxide – urea method.