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(2,6-dimethyl-1,3-dioxan-4-yl) acetate

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Identification
Molecular formula
C9H14O4
CAS number
6972-64-9
IUPAC name
(2,6-dimethyl-1,3-dioxan-4-yl) acetate
State
State

It is typically found in a liquid state at room temperature.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
190.50
Boiling point (Kelvin)
463.70
General information
Molecular weight
186.21g/mol
Molar mass
186.2110g/mol
Density
1.0210g/cm3
Appearence

(2,6-dimethyl-1,3-dioxan-4-yl) acetate is a colorless liquid with a sweet, fruity odor. It is commonly used as a fragrance and flavoring agent in various applications.

Comment on solubility

Solubility of (2,6-dimethyl-1,3-dioxan-4-yl) acetate

(2,6-dimethyl-1,3-dioxan-4-yl) acetate is an organic compound that exhibits interesting solubility characteristics. The solubility of this compound can be influenced by several factors, such as its molecular structure and the polarity of the solvent.

Factors Affecting Solubility:

  • Molecular Structure: The presence of the dioxane ring and the acetate functional group contributes to both the polar and non-polar characteristics of the compound.
  • Polarity of Solvent: (2,6-dimethyl-1,3-dioxan-4-yl) acetate is likely to be soluble in polar solvents like water and alcohols due to its polar functional groups. However, it may also exhibit some solubility in non-polar solvents.

In general, organic compounds with similar functional groups tend to exhibit comparable solubility behaviors. As a rule of thumb, "like dissolves like" applies: polar solvents will dissolve polar solutes more effectively than non-polar solutes.

To summarize, (2,6-dimethyl-1,3-dioxan-4-yl) acetate should demonstrate reasonable solubility in polar solvents, reflecting the dual nature of its molecular structure. This solubility behavior allows it to interact in various chemical environments, making it a versatile compound in chemical reactions.

Interesting facts

Interesting Facts about (2,6-Dimethyl-1,3-Dioxan-4-yl) Acetate

(2,6-Dimethyl-1,3-dioxan-4-yl) acetate is a compound that belongs to the class of esters, specifically formed from the reaction of an acid and an alcohol. This compound is particularly fascinating due to its unique structural features and potential applications.

Chemical Structure

The structural architecture of (2,6-Dimethyl-1,3-dioxan-4-yl) acetate is distinguished by:

  • Dioxane Ring: The presence of a dioxane ring lends the compound notable stability and contributes to its reactive properties.
  • Dimethyl Substituents: The dimethyl groups enhance the lipophilicity, which can be beneficial in various chemical reactions and applications.
  • Acetate Functional Group: The acetate moiety imparts useful characteristics, making this compound suitable for various synthesis pathways.

Applications

This compound holds promise in several domains, example applications include:

  • Solvents: Its unique properties can be harnessed as an effective solvent in organic reactions.
  • Flavor and Fragrance Industry: Compounds with acetate groups are often found in synthetic flavors and fragrances, adding to their sweetness and complexity.
  • Pharmaceuticals: The incorporation of similar structures into drug design serves to enhance bioactivity and stability.

Research Potential

Due to its unique composition, (2,6-Dimethyl-1,3-dioxan-4-yl) acetate is a valuable subject for further study. Researchers are interested in:

  • Exploring its reactivity in synthetic organic chemistry.
  • Investigating its potential as a precursor for functional materials.
  • Understanding its behavior in biochemical processes, with the aim to develop targeted drug releases.

In conclusion, (2,6-Dimethyl-1,3-dioxan-4-yl) acetate exemplifies the complexity and versatility found within organic chemistry. Its unique structural features and multifaceted applications make it an intriguing compound worthy of study and exploration.

Synonyms
DIMETHOXANE
828-00-2
Acetomethoxane
1,3-Dioxan-4-ol, 2,6-dimethyl-, acetate
GIV Gard DXN
GIV Gard DXN-CO
G1V Gard DXN
Caswell No. 363
Dioxin CO
2,6-Dimethyl-1,3-dioxan-4-ol acetate
NCI-C56213
6-Acetoxy-2,4-dimethyl-m-dioxane
Dioxin (bactericide)
2,4-Dimethyl-6-m-dioxanyl acetate
CCRIS 246
Dioxin (bactericide) (Obs.)
2,6-Dimethyl-m-dioxan-4-ol acetate
2,6-Dimethyl-m-dioxan-4-yl acetate
Acetomethoxan
2,4-Dimethyl-6-acetoxy-1,3-dioxane
6-Acetoxy-2,4-dimethyl-1,3-dioxane
HSDB 4311
m-Dioxan-4-ol, 2,6-dimethyl-, acetate
EINECS 212-579-9
UNII-S0859MSI8I
6-Acetoxy-2,4-dimethyl-meta-dioxane
EPA Pesticide Chemical Code 001001
Acetic acid, 2,6-dimethyl-m-dioxan-4-yl ester
2,6-Dimethyl-meta-dioxan-4-ol acetate
2,6-Dimethyl-meta-dioxan-4-yl acetate
BRN 0128710
S0859MSI8I
DTXSID6020480
AI3-51032
DIMETHOXANE [MI]
DIMETHOXANE [HSDB]
DIMETHOXANE [IARC]
2,6-Dimethyl-1,3-dioxan-4-yl acetat
Acetic acid, ester with 2,6-dimethyl-m-dioxan-4-ol
DTXCID00480
1,3-Dioxan-4-ol, 2,6-dimethyl-, 4-acetate
2,6-Dimethyl-1,3-dioxan-4-yl acetat [IUPAC]
4-19-00-00641 (Beilstein Handbook Reference)
Dioxan-4-ol, 2,6-dimethyl-, acetate
DIMETHOXANE (IARC)
2,6-Dimethyl-m-dioxan-4-yl ester acetic acid
2,6-Dimethyl-1,3-dioxan-4-yl acetat (IUPAC)
GIV Gard DXNCO
6Acetoxy2,4dimethylmdioxane
2,4Dimethyl6mdioxanyl acetate
2,6Dimethylmdioxan4ol acetate
2,6Dimethylmdioxan4yl acetate
6Acetoxy2,4dimethylmetadioxane
2,4Dimethyl6acetoxy1,3dioxane
6Acetoxy2,4dimethyl1,3dioxane
2,6Dimethylmetadioxan4ol acetate
2,6Dimethylmetadioxan4yl acetate
2,6Dimethyl1,3dioxan4ol acetate
mDioxan4ol, 2,6dimethyl, acetate
1,3Dioxan4ol, 2,6dimethyl, acetate
Acetic acid, 2,6dimethylmdioxan4yl ester
1,3-DIOXAN-4-OL, 2-6-DIMETHYL-, ACETATE
212-579-9
phmnxpygvpeqsj-uhfffaoysa-n
un3272
Dimethoxane, commercial grade
2,6-Dimethyl-1,3-dioxan-4-yl acetate
CHEBI:82450
Ddoa
(2,6-dimethyl-1,3-dioxan-4-yl) acetate
CAS-828-00-2
SCHEMBL8937
CHEMBL1484947
6-Acetoxy-2,4-dimethyl-m-dioxan
2,6-dimethyl-m-dioxan-4-olacetate
Tox21_202123
Tox21_300414
AKOS015913410
NCGC00090862-01
NCGC00090862-02
NCGC00090862-03
NCGC00090862-04
NCGC00254247-01
NCGC00259672-01
2,6-Dimethyl-1,3-dioxan-4-yl acetate #
NS00007523
C19402
Q26840787