Interesting facts
Interesting Facts about 2,2-Dimethyl-1,3-Dioxane-4,6-Dione
2,2-dimethyl-1,3-dioxane-4,6-dione is a fascinating compound with a variety of applications and interesting structural characteristics. Here are some engaging insights about this unique molecule:
- Structural Intricacies: This compound features a dioxane ring, which is known for its cyclic nature and the ability to stabilize various functional groups. The presence of two carbonyl (C=O) groups in its structure adds to its reactivity and versatility.
- Role in Synthetic Chemistry: Often used as an intermediate in the synthesis of more complex organic compounds, 2,2-dimethyl-1,3-dioxane-4,6-dione plays a vital role in drug development and the production of agrochemicals. Its reactivity can be harnessed to create diverse derivatives.
- Biological Relevance: Some derivatives of dioxane compounds exhibit biological activity, making them of interest for pharmaceutical applications. Research into the bioactivity of 2,2-dimethyl-1,3-dioxane-4,6-dione's derivatives is ongoing, potentially leading to novel therapeutic agents.
- Synthesis Techniques: The synthesis of 2,2-dimethyl-1,3-dioxane-4,6-dione showcases various organic synthesis techniques, including the formation of dioxane rings through acid-catalyzed reactions, highlighting the creative processes chemists employ to construct complex molecules.
As chemists continue to explore and refine their understanding of such compounds, the implications in both industry and academia are boundless. A deep understanding of these compounds not only enhances our knowledge of organic chemistry but also contributes to innovative solutions across multiple scientific fields.
Synonyms
2,2-Dimethyl-1,3-dioxane-4,6-dione
Meldrum's acid
1,3-Dioxane-4,6-dione, 2,2-dimethyl-
Isopropylidene malonate
Meldrums acid
2,2-Dimethyl-1,3-dioxan-4,6-dione
Cyclic isopropylidene malonate
Malonic acid, cyclic isopropylidene ester
2,2-Dimethyl-m-dioxane-4,6-dione
2,2-Dimethyl-4,6-dioxo-m-dioxane
MELDRUMIC ACID
NSC 71902
AI3-39039
UNII-DD139RP1SC
EINECS 217-992-8
DD139RP1SC
m-DIOXANE-4,6-DIONE, 2,2-DIMETHYL-
2,2-dimethyl-4,6-dioxo-1,3-dioxane
BRN 0117310
NSC-71902
NSC-688343
2,2-PROPANEDIOL CYCLIC MALONATE
MELDRUM'S ACID [MI]
DTXSID7051846
EC 217-992-8
5-19-05-00008 (Beilstein Handbook Reference)
4,6-Diketo-2,2-dimethyl-1,3-dioxane
2,2Dimethyl4,6dioxomdioxane
2,2Dimethylmdioxane4,6dione
DTXCID5030402
mDioxane4,6dione, 2,2dimethyl
2,2Dimethyl1,3dioxane4,6dione
1,3Dioxane4,6dione, 2,2dimethyl
Malonic acid, cyclic isopropylidene ester (8CI)
gxhfuvwignlzsc-uhfffaoysa-n
inchi=1/c6h8o4/c1-6(2)9-4(7)3-5(8)10-6/h3h2,1-2h
2033-24-1
Malonic acid cyclic isopropylidene ester
MFCD00006638
cycl-Isopropylidene malonate
NSC688343
2,2-dimethyl-[1,3]dioxane-4,6-dione
MELDRUM ACID
Meidrum's Acid
Meldrum\'s acid
2,6-dione
2,6-dioxo-m-dioxane
SCHEMBL5976
1,6-dione, 2,2-dimethyl-
m-Dioxane-4, 2,2-dimethyl-
N,N-Dimethyl-1-4-aminobilidine
ALBB-013484
CS-D1154
Dimethyl-[1,3]dioxane-4,6-dione
HY-Y0232
NSC71902
STR00259
CX1199
STK397458
2,2-dimethyl-1,3-dioxane-4,6dione
2,2-dimethyl-1,3-dioxane4,6-dione
2,2dimethyl-1,3-dioxane-4,6-dione
AKOS000119035
AB00787
AC-2044
FC04271
2,2 dimethyl-1,3 dioxane-4,6 dione
2.2-dimethyl-1,3-dioxane-4,6-dione
2.2-dimethyl-[1,3]dioxane-4,6-dione
SY001708
2, 2-dimethyl-1,3-dioxane-4, 6-dione
2,2-dimethyl-[1,3]-dioxan-4,6-dione
2,2-dimethyl-[1,3]-dioxane-4,6-dione
M0799
NS00005683
EN300-19266
2,2-Dimethyl-1,3-dioxane-4,6-dione, 98%
Q421283
2,2-Dimethyl-1,3-dioxane-4,6-dione;Meldrum's acid
F3096-1700
Malonic acid cyclic isopropylidene ester, Meldrum's acid, cycl-Isopropylidene malonate
Solubility of 2,2-dimethyl-1,3-dioxane-4,6-dione
The solubility of 2,2-dimethyl-1,3-dioxane-4,6-dione is a fascinating topic due to its unique structural properties. This compound, often referred to as dimethyl dioxane, features a dioxane ring that influences its solubility characteristics significantly.
Key Points About Solubility:
In summary, the solubility of 2,2-dimethyl-1,3-dioxane-4,6-dione is significantly influenced by its chemical structure, particularly its polarity and size of substituents. Its aqueous solubility makes it a versatile compound in various applications, emphasizing the importance of understanding solubility in the study and application of chemical compounds.