Interesting facts
Interesting Facts about 2-(1,3-Dioxoisoindolin-2-yl)acetic Acid
2-(1,3-Dioxoisoindolin-2-yl)acetic acid is a fascinating compound that bridges several fields, from organic chemistry to pharmacology. Here are some intriguing insights into this compound:
- Structural Diversity: This compound features a unique isoindole framework, which contributes to its vast array of biological activities. The presence of the dioxo group enhances its reactivity and stability.
- Pharmacological Potential: Compounds with similar structures have been studied for their roles in various therapeutic applications, including anti-inflammatory and anti-cancer properties. Research indicates that derivatives of this compound may exhibit significant biological activity.
- Synthetic Routes: The synthesis of 2-(1,3-dioxoisoindolin-2-yl)acetic acid offers a spectacular case study in organic synthesis, demonstrating the interplay of different reaction mechanisms, such as condensation and cyclization.
- Applications: Beyond pharmacology, the unique characteristics of this compound make it a candidate for applications in materials science, particularly in the development of organic semiconductors or light-emitting systems.
In the words of a noted chemist, "The beauty of organic synthesis lies in the exploration of structures that nature rarely makes, but that we can create through our understanding of chemistry." This phrase underscores the potential for creativity and discovery inherent in the study of compounds like 2-(1,3-dioxoisoindolin-2-yl)acetic acid. Advances in research may one day unlock more secrets of this compound, paving the way for new innovations in science and medicine.
Synonyms
N-Phthaloylglycine
4702-13-0
Phthalimidoacetic acid
N-Phthalylglycine
N-(Carboxymethyl)phthalimide
Phthaloylglycine
N,N-Phthaloylglycine
N-Phthalylglycin
2H-Isoindole-2-acetic acid, 1,3-dihydro-1,3-dioxo-
1,3-Dioxo-2-isoindolineacetic acid
PHTHALOYL GLYCINE
2-ISOINDOLINEACETIC ACID, 1,3-DIOXO-
2-phthalimidoacetic acid
EINECS 225-177-3
6J5LY4N0CG
NSC 10771
NSC 29044
BRN 0184174
1,3-Dihydro-1,3-dioxo-2H-isoindole-2-acetic acid
NSC-10771
NSC-29044
PHTHALYLGLYCINE, N-
DTXSID00197005
5-21-10-00430 (Beilstein Handbook Reference)
DTXCID70119496
2H-Isoindole-2-acetic acid, 1,3-dihydro-1,3-dioxo-(9CI)
inchi=1/c10h7no4/c12-8(13)5-11-9(14)6-3-1-2-4-7(6)10(11)15/h1-4h,5h2,(h,12,13
PHTHALOYL-GLYCINE
(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)acetic acid
2-(1,3-dioxoisoindolin-2-yl)acetic acid
2-(1,3-Dioxo-2,3-Dihydro-1H-Isoindol-2-Yl)Acetic Acid
MFCD00005900
(1,3-dioxoisoindol-2-yl)acetic acid
2-(1,3-dioxoisoindol-2-yl)acetic acid
2-Isoindolineacetic acid,3-dioxo-
2H-Isoindole-2-acetic acid,3-dihydro-1,3-dioxo-
UNII-6J5LY4N0CG
51X
Phthalyl-dl-glycine
2phthalimidoacetic acid
N-Phthalimidoacetic Acid
ChemDiv2_003427
N-Phthaloylglycine, 97%
Oprea1_318928
CBDivE_001696
SCHEMBL522649
CHEMBL2429920
BDBM16417
HMS1378L17
ALBB-000314
NSC10771
NSC29044
CCG-15120
STK057081
AKOS000119369
CS-W015381
FD21597
HY-W014665
PS-5757
N-Phthaloylglycine Phthalimidoacetic acid
AC-18321
NS00031658
P0963
EN300-16561
N-Phthaloylglycine, puriss., >=99.0% (T)
AE-641/02488025
SR-01000389673
SR-01000389673-1
(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-acetic acid
Q27264991
Z56175684
F0266-0673
(1,3-DIOXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)-ACETIC ACID
N-phthalimidoacetic acid;2-(1,3-dioxoisoindolin-2-yl)acetic acid
Solubility of 2-(1,3-dioxoisoindolin-2-yl)acetic acid
The solubility of 2-(1,3-dioxoisoindolin-2-yl)acetic acid is an intriguing aspect of its chemical behavior. This compound features complex functional groups that can significantly influence its solubility profile. Here are some key points to consider:
Experimental data is crucial for confirming these solubility behaviors, as theoretical predictions can only suggest trends. Overall, understanding the solubility characteristics of 2-(1,3-dioxoisoindolin-2-yl)acetic acid can provide valuable insight for its applications and interactions in various environments.