Interesting facts
Interesting Facts about 2,2-Dimethylpropanoyl 2,2-Dimethylpropanoate
2,2-Dimethylpropanoyl 2,2-dimethylpropanoate is a fascinating compound that showcases the intricacies of organic chemistry. This ester is part of a group known for its diverse applications and reactivity patterns. Here are some interesting aspects about this compound:
- Functional Group: As an ester, it features the characteristic -COO- linkage, which is crucial in many biological and industrial processes. Esters are often responsible for the pleasant fragrances found in fruits.
- Applications: Compounds like 2,2-dimethylpropanoyl 2,2-dimethylpropanoate find use in various fields, including:
- Flavorings and Fragrances: Its unique structure may contribute to flavor profiles in food products.
- Synthesis: Acts as an intermediate in organic synthesis, connecting other functional groups.
- Potential Medicinal Applications: Like many esters, it could be explored for pharmaceutical uses.
- Chemical Behavior: Esters, including this compound, are known for their role in condensation reactions and can undergo hydrolysis to yield acids and alcohols, a process important in both laboratory and chemical manufacturing settings.
- Isomerism: The presence of multiple methyl groups in the molecule contributes to potential stereochemistry, making its study vital for understanding different structural configurations.
- Environmental Impact: As with many chemicals, the application and disposal of 2,2-dimethylpropanoyl 2,2-dimethylpropanoate must be managed carefully to minimize environmental concerns, emphasizing the need for responsible chemical practices.
- Laboratory Handling: Working with this compound requires standard safety precautions as with all organic compounds, highlighting the importance of safety in chemical experimentation.
Overall, 2,2-dimethylpropanoyl 2,2-dimethylpropanoate serves as a compelling example of the diverse and applicable nature of esters in organic chemistry. The compound not only sparks interest due to its structural characteristics but also for its potential in various scientific disciplines.
Synonyms
Trimethylacetic anhydride
Pivalic anhydride
1538-75-6
Propanoic acid, 2,2-dimethyl-, anhydride
EINECS 216-263-1
DTXSID601014577
Propanoic acid, 2,2-dimethyl-, 1,1'-anhydride
2,2Dimethylpropionic anhydride
DTXCID00818566
Propanoic acid, 2,2dimethyl, anhydride
Propanoic acid, 2,2dimethyl, 1,1'anhydride
216-263-1
2,2-dimethylpropanoyl 2,2-dimethylpropanoate
2,2-Dimethylpropionic anhydride
2,2-Dimethylpropanoic anhydride
MFCD00008842
Trimethylacetic Anhydride1538-75-6
Pivalicanhydride
Pivalic anydride
Piv2O
pivalic acid anhydride
SCHEMBL65267
Trimethylacetic anhydride, 99%
2,2,2-trimethylacetic anhydride
PGZVFRAEAAXREB-UHFFFAOYSA-
TRIMETHYL ACETIC ANHYDRIDE
1,1-Dimethylpropanoic anhydride #
BCP22749
2,2-dimethylpropanoic acid anhydride
2,2-dimethylpropionic acid anhydride
AKOS005258332
BP-30106
DA-20896
MS-20247
PD065632
2,2-dimethylpropanoyl2,2-dimethylpropanoate
CS-0154934
NS00047573
P1414
D92125
EN300-1692861
A809474
F0001-0547
2,2-dimethylpropanoic acid (2,2-dimethyl-1-oxopropyl) ester
InChI=1/C10H18O3/c1-9(2,3)7(11)13-8(12)10(4,5)6/h1-6H3
Solubility of 2,2-dimethylpropanoyl 2,2-dimethylpropanoate
The solubility of 2,2-dimethylpropanoyl 2,2-dimethylpropanoate can be characterized as follows:
In summary, while 2,2-dimethylpropanoyl 2,2-dimethylpropanoate may have limited solubility in polar solvents, its performance in organic environments is typically more favorable, demonstrating that like dissolves like. For applications requiring this compound, considering the choice of solvent will be essential to achieve the desired solubility.