Interesting facts
Interesting Facts about Isoindoline-1,3-dione
Isoindoline-1,3-dione, also known as phthalimide, is a fascinating compound with a rich history in organic chemistry. It is often viewed as a versatile building block for various synthesis processes, especially in the pharmaceutical industry. Here are some engaging facts about this intriguing compound:
- Structural Significance: Isoindoline-1,3-dione features a unique bicyclic structure that contributes to its reactivity and applicability in organic reactions. The presence of two functional groups adds to its versatility.
- Applications in Synthesis: This compound is widely used as a precursor in the synthesis of numerous important pharmaceuticals, particularly those exhibiting therapeutic properties. For instance, it has been employed in creating medications for treating various ailments.
- Role in 'Green Chemistry': Isoindoline-1,3-dione serves as a valuable reagent in reactions promoting environmentally friendly practices. As a result, it has garnered attention for its role in reducing waste and improving reaction efficiency.
- Research Interest: Due to its interesting pharmacological properties, this compound is the subject of ongoing research. Scientists are exploring its potential as a lead compound for developing new drugs, targeting a wide range of biological activities.
- Photocatalytic Properties: Isoindoline-1,3-dione has shown promise in photocatalytic processes, which harness light energy to drive reactions. This characteristic adds another layer of utility to its chemical profile.
In summary, isoindoline-1,3-dione is not just a simple compound; it is a gateway to innovations in synthesis and drug development. Its diverse applications and ongoing research potential make it a significant subject for chemists and pharmaceutical professionals alike.
Synonyms
PHTHALIMIDE
85-41-6
Isoindole-1,3-dione
1H-Isoindole-1,3(2H)-dione
O-Phthalimide
o-Phthalic imide
isoindoline-1,3-dione
Benzoimide
1,3-Isoindolinedione
2-Diazoindan-1,3-dione
Phenylimide
Phthalimid
1,2-Benzenedicarboximide
Ftalimmide
2,3-dihydro-1H-isoindole-1,3-dione
phtalimide
1,3-Isoindoledione
NSC 3108
Phthalic dicarboximide
HSDB 5007
1,3-Dihydroisoindole-1,3-dione
EINECS 201-603-3
UNII-1J6PQ7YI80
BRN 0118522
1J6PQ7YI80
CCRIS 9479
DTXSID3026514
CHEBI:38817
AI3-07565
NSC-3108
DTXCID506514
EC 201-603-3
5-21-10-00270 (Beilstein Handbook Reference)
MFCD00005881
Phthalimid [German]
Ftalimmide [Italian]
CAS-85-41-6
136918-14-4
223537-84-6
Phthalimide; Tafenoquine related; SKF-2450
1,3-Dihydro-1,3-dioxoisoindole
isoindoledione
Pthalimide
phthalimide-
hydroxyisoindolone
folpet TP1
hydroxy isoindolone
1,3-dioxoisoindole
isoindol-1,3-dione
isoindoline-1,3 dione
Phthalimide, >=99%
3-hydroxyisoindol-1-one
SCHEMBL64
isoindoline -1,3-dione
PHTHALIMIDE [MI]
1h-isoindole-1,3-dione
PHTHALIC ACID,IMIDE
WLN: T56 BVMVJ
isoindole-1,3(2H)-dione
1H-isoindole-1,3(2H)dione
3-Hydroxy-1H-isoindol-1-one
CHEMBL277294
1H-isoindole-1,3(2H) dione
1H-isoindol-1,3-(2H)-dione
NSC3108
1H-isoindole-1,3-(2H)-dione
isoindoline-1,3-dione;Phthalimide
BCP21906
Tox21_201800
Tox21_303319
BBL037023
BDBM50350644
STK299439
2,3-dihydro-1H-isoindole-1,3-dion
AKOS000119824
1,3-Dihydro-2H-isoindole-1,3-dione
FP31525
FS-3820
NCGC00249121-01
NCGC00257137-01
NCGC00259349-01
Phthalimide, puriss., >=99.0% (T)
DS-002743
phthalimide [1h-isoindole-1,3(2h)-dione]
NS00010682
P0402
EN300-17966
P60059
Phthalimide, PESTANAL(R), analytical standard
A841324
AP-770/40217754
Q412784
Z57127356
F9995-1638
Phthalic dicarboximide; Phthalimide; Isoindole-1,3-dione
InChI=1/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11
201-603-3
Solubility of Isoindoline-1,3-dione
Isoindoline-1,3-dione, with the molecular formula C8H5NO2, exhibits varying solubility characteristics depending on the solvent used. Understanding its solubility profile is essential for applications in organic synthesis and pharmaceuticals.
Characteristics of Solubility:
This compound is classified as having moderate solubility in organic solvents but can be challenging when attempting to dissolve in water or alcohols. To quote one study, "the solubility behaviors can significantly impact the compound's reactivity and usability in various chemical reactions." Thus, choosing the right solvent is crucial for optimizing its applications.
Overall, isoindoline-1,3-dione demonstrates interesting solubility traits that are vital for anyone working with this compound. Understanding and leveraging these solubility properties can lead to better outcomes in synthesis and application.