Interesting facts
Interesting Facts About Tetrahydrofuran-2,5-dione
Tetrahydrofuran-2,5-dione, commonly referred to as THF-dione, is an intriguing compound that has captured the interest of chemists and researchers alike. Here are some captivating highlights:
- Structure and Stability: The unique cyclic structure of THF-dione contributes to its stability under a variety of conditions, making it an excellent candidate for further chemical reactions.
- Role in Synthesis: THF-dione is widely used as a building block in organic synthesis, particularly in the production of biologically active compounds and pharmaceuticals. Its ability to participate in reactions is vital for developing new materials.
- Versatile Reactivity: This compound exhibits reactivity towards nucleophiles, leading to significant functional group transformations. Its versatility makes it an essential tool in the organic chemist's arsenal.
- Research Applications: THF-dione is being researched for its potential applications in polymer science and the development of novel chemical materials, showcasing its importance in cutting-edge scientific studies.
"Chemistry is not just about molecules and compounds; it's about understanding the connections that bind them together. Tetrahydrofuran-2,5-dione embodies this philosophy through its diverse applications and reactions."
As you explore the world of organic compounds, keep an eye on THF-dione—it represents the beauty and complexity of chemical structures and their invaluable roles in science and technology.
Synonyms
SUCCINIC ANHYDRIDE
108-30-5
dihydrofuran-2,5-dione
oxolane-2,5-dione
Succinic acid anhydride
Succinyl oxide
Dihydro-2,5-furandione
2,5-Diketotetrahydrofuran
Succinyl anhydride
Butanedioic anhydride
Rikacid SA
2,5-Furandione, dihydro-
Tetrahydro-2,5-dioxofuran
2,5-Dioxotetrahydrofuran
Tetrahydro-2,5-furandione
Bernsteinsaure-anhydrid
NCI-C55696
Dihydro-furan-2,5-dione
NSC 8518
MFCD00005525
CCRIS 2386
HSDB 792
Dihydro-2,5-diketotetrahydrofuran
EINECS 203-570-0
UNII-6RF4O17Z8J
BRN 0108441
6RF4O17Z8J
Bernsteinsaeureanhydrid
DTXSID7021287
CHEBI:36595
AI3-52664
SuccinicAnhydride-13C4
NSC-8518
2,5(3H,4H)-Furandione
Succinic anhydride treated BSA
DTXCID701287
EC 203-570-0
5-17-11-00006 (Beilstein Handbook Reference)
Succinyloxide
SUCCINIC ANHYDRIDE (IARC)
SUCCINIC ANHYDRIDE [IARC]
Bernsteinsaure-anhydrid [German]
tetrahydrofuran-2,5-dione
2, dihydro-
EINECS 270-161-1
Oxolan-2,5-dione
WLN: T5VOVTJ
butanedioic acid anhydride
Dihydro-2, 5-furandione
Succinic anhydride, 97%
BERNSTEINSAUREANHYDRID
tetrahydro-furan-2,5-dione
Tetrahydro-2, 5-dioxofuran
SCHEMBL16123
MLS002454448
SUCCINIC ANHYDRIDE [MI]
CHEMBL1370164
NSC8518
SUCCINIC ANHYDRIDE [HSDB]
HMS3039B10
STR01303
Succinic anhydride, >=99% (GC)
Tox21_201179
STL194303
AKOS000121191
FS37926
Succinic anhydride, >=97.0% (NT)
NCGC00091291-01
NCGC00091291-02
NCGC00258731-01
BP-13070
CAS-108-30-5
HY-79369
SMR001372026
DB-042683
DB-050501
Butanedioic acid,anhydride succinic anhydride
CS-0011581
NS00003241
S0107
EN300-18021
C19524
D78120
Succinic anhydride, puriss., >=99.0% (NT)
Succinic anhydride, SAJ first grade, >=99.0%
A801840
Q417847
BUTANEDIOIC ACID,ANHYDRIDE SUCCINIC ANHYDRIDE
Z57127506
F1908-0090
InChI=1/C4H4O3/c5-3-1-2-4(6)7-3/h1-2H
203-570-0
Tetrahydro-2,5-furandione(National Library of Medicine, SIS; ChemIDplus Record for Succinic anhydride (108-30-5) Available from, as of July 21, 2005: http://chem.sis.nlm.nih.gov/chemidplus/chemidlite.jsp)
Solubility of Tetrahydrofuran-2,5-dione
Tetrahydrofuran-2,5-dione, commonly known as 2,5-diketotetrahydrofuran, exhibits interesting solubility characteristics due to its unique molecular structure. This compound is known for its ability to dissolve in a variety of solvents, making it versatile for different applications.
Solubility Features:
As noted in various studies, the solubility behavior of tetrahydrofuran-2,5-dione can be summarized as:
In summary, the solubility of tetrahydrofuran-2,5-dione is a critical factor that influences its utility in chemical reactions and formulations. Its ability to dissolve in both polar and non-polar solvents enhances its functionality in various chemical processes.